PulpitisNCT03168620
Effect of Glass Ionomer Cement as an Interim Restoration in Diagnosis of Pulpal Status
A study testing Restoration in people with Pulpitis, run by Postgraduate Institute of Dental Sciences Rohtak.
Trial summary
Aim: To evaluate whether glass ionomer interim therapeutic restoration (ITR) in asymptomatic teeth with deep cavities can help in determining the pulp status. Methodology: 146 mandibular molars with deep carious lesion having positive response to pulp sensitivity were randomly allocated to two study groups (75-ITR… Read more about this study
- Who is it for?
- Ages 15 to 54 yearsHealthy volunteers can take part
- Conditions the study is for
- Pulpitis
- What is being tested?
- Restoration
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 146 participants
- Where
- No sites listed yet
- Study dates
- 20 May 2015to 30 Nov 2016
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 15 to 54 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- mature permanent mandibular molars having deep carious lesions involving half or more of the dentine detected by radiographic examination,
- pulp sensibility confirmed using the electric pulp test (Digitest D626D; Parkell Electronics, New York, NY) and the cold test (Endo frost, Coltene, Whaledent),
- absence of apical and furcal radiolucency determined by radiographic examination,
- absence of clinical symptoms of irreversible symptoms, fistula, swelling and abnormal tooth mobility.
- Clinical diagnosis of vital pulp was made on the basis of radiographic and clinical examination and the pulp sensibility tests.
- Exclusion Criteria:• if they presented with signs and symptoms of irreversible pulpitis,
Show all 10Show fewer
- had negative response to vitality tests before or after ITR,
- diabetic, immunocompromised,
- pregnant,
- had a positive history of antibiotic use in past one month or required antibiotic prophylaxis.
Who cannot join
None listed.
About this study
Official title: Evaluation of the Effect of Glass Ionomer Cement as an Interim Restoration in Diagnosis of Pulpal Status in Permanent Teeth: A Prospective Randomized Clinical Trial
Aim: To evaluate whether glass ionomer interim therapeutic restoration (ITR) in asymptomatic teeth with deep cavities can help in determining the pulp status. Methodology: 146 mandibular molars with deep carious lesion having positive response to pulp sensitivity were randomly allocated to two study groups (75-ITR, 71- NON-ITR group). In the first group after partial caries removal(PCR), interim therapeutic restoration of glass ionomer cement (GIC) Ketac molar was placed for one month before definitive adhesive restoration. In NON-ITR group, cavity preparation was similar to ITR group, but definitive restoration was done in the same visit. Two examiners evaluated the clinical and radiographic outcomes for 18 months. Success was defined as absence of signs and symptoms of irreversible pulpitis and absence of periapical alterations.
Read the detailed description
Introduction Preservation of pulp vitality while managing the deep carious lesions is often a great challenge and requires procedures like pulp capping and pulpotomy collectively termed as vital pulp therapy (VPT). Such treatment involves elimination of bacteria from pulp dentine complex and establishing an environment that will prevent any future bacterial contamination and improves survival prognosis. Management of deep carious lesions in recent years has changed from complete caries removal to partial caries removal. Partial caries removal has gained importance due to reduction in pulpal exposures, less postoperative complications, more preservation and maintenance of pulp tissue .
The important concern during VPT is accurate assessment of pulpal status. Methods to determine pulpal vitality include patient history, signs and symptoms, radiographs and pulp sensibility tests. One of the hallmarks of pulpal diagnosis is that it is difficult and has a high rate of inaccuracy. Pain on cold and hot stimuli cannot be considered as a reliable reference for making a treatment decision. Also insufficient evidence was found to determine the diagnostic accuracy of symptoms, signs, and diagnostic tests to assess the pulp status.
Studies using visual and histological inspection of exposed pulp to examine status of pulp reported marked variation in sensitivity of cold and electric pulp test from 0 .21 to 0.94, with relatively less variation in specificity from 0.73 to 0 .96.Sensitivity decreased to 67% when the spectrum of the disease was altered i.e. when asymptomatic teeth with deep carious lesions were included . Diagnosis of pulp status is often easy when there is a clear distinction between healthy and necrosed pulp however it is more difficult in asymptomatic teeth with deep carious lesions.
Recently, Coll et al. proposed that glass ionomer cement (GIC) as interim therapeutic restoration (ITR) improved pulpal diagnosis and VPT outcomes while interpreting diagnostic assessment based on clinical pulp therapy success. Vij et al. reported that GIC temporization for 1-3 months increased success of the subsequent VPT from 79% to 92% .However; both of the studies were retrospective and were in deciduous teeth.
No prospective clinical study has so far been conducted in permanent teeth that demonstrate the effectiveness of GIC and other adhesive restoration materials in determining the pulpal status. Aim of this double blinded randomized controlled trial was to assess the effectiveness of GIC interim restoration in determining the pulpal status of asymptomatic teeth with deep carious lesions. Null hypothesis was that GIC as ITR does not improve the clinician's diagnostic ability to determine the correct pulp clinical diagnosis and does not improve the treatment outcomes in vital pulp therapy.
Material and Methods:
Case Selection This prospective randomized clinical trial was conducted at the Department of Conservative Dentistry and Endodontics, Post Graduate Institute of Dental Sciences, Rohtak, India. The study protocol was approved by the Ethical Committee (PGIDS/IEC/2015/64) of the Post Graduate Institute of Dental Sciences. A total of 146 patients were included with an age range of 15-54 years. The inclusion criteria for the study were: 1) mature permanent mandibular molars having deep carious lesions involving half or more of the dentine detected by radiographic examination, 2) pulp sensibility confirmed using the electric pulp test (Digitest D626D; Parkell Electronics, New York, NY) and the cold test (Endo frost, Coltene, Whaledent), 3) absence of apical and furcal radiolucency determined by radiographic examination, 4) absence of clinical symptoms of irreversible symptoms, fistula, swelling and abnormal tooth mobility. Clinical diagnosis of vital pulp was made by the chief supervisor (Sanjay Tewari) on the basis of radiographic and clinical examination and the pulp sensibility tests. Patients were excluded if they presented with signs and symptoms of irreversible pulpitis, had negative response to vitality tests before or after ITR, diabetic, immunocompromised, pregnant, or had a positive history of antibiotic use in past one month or required antibiotic prophylaxis. Informed consent explaining benefits and risks of treatment was taken from patients before participation in the trial.
Sample Size Calculation and Randomization The sample size calculation was done on the basis of difference in the percentage of success of vital pulp therapy using GIC (98%) versus non-GIC group (75%) (12) α=5% with a power of 90%. This indicated the need for 48 restorations per treatment group. Given an expected attrition rate of 20%, 60 teeth were included in each treatment group. Randomization was developed to eliminate any bias on the part of the investigators and to equalize the number of patients between the 2 treatment groups. Using an equal proportion randomization allocation ratio, one of the investigators (M.J) created envelopes containing concealed assignment codes that were assigned sequentially to eligible patients.
Clinical Procedure The procedure was performed under local anesthesia and rubber dam isolation. Carious tissue from the lateral walls and dentinoenamel junction was removed completely by using low-speed metal burs and/or hand excavator. Superficial necrotic dentin was removed from the pulpal and axial wall using low speed round bur. A layer of soft, wet carious dentin was left adjacent to pulpal wall. The cavity was cleaned with distilled water and dried with sterile filter paper. In group ITR, the cavity was filled with GIC ( Ketac Molar (3M ESPE, St. Paul, Minn., USA).Cavity was reopened after 1 months in asymptomatic patients , restoration was removed completely ,base of resin modified glass ionomer cement(RMGIC) (Fuji Lining LC;GC,Tokyo,Japan)was applied and cavity was restored with resin composite(Tetric N-Ceram;Ivoclar Vivadent) according to manufacturer instructions.
In NON-ITR group, cavity preparation was done similar to ITR group, after partial caries excavation ,base of RMGIC (Fuji Lining LC;GC,Tokyo,Japan) was applied and all cavities were restored with resin composite(Tetric N-Ceram;Ivoclar Vivadent) according to manufacturer instructions.
Outcome Assessment Two blinded examiners assessed the clinical and radiographic outcomes of test and control treatments at 1, 3, 6, 12, 18 months after treatment. Success was defined as absence of signs and symptoms of irreversible pulpitis (spontaneous pain, fistula and swelling), positive response to pulp sensibility tests and absence of periapical alterations (radiolucency at furcal or periapical region, calcification) (combined outcome). Pretreatment pulpal diagnosis was considered successful when teeth treated with or without ITR were diagnosed as vital and none of clinical and radiographic signs and symptoms of failure developed during 18 month follow up.
- Conditions
- Pulpitis
- Being tested
- Restoration
- Medical subject headings
- Pulpitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
RestorationProcedure or surgery
Also called Filling
| Study group | Role | What they receive |
|---|---|---|
| ITR group | Active comparator | In ITR group after partial caries removal(PCR), interim therapeutic restoration of glass ionomer cement (GIC) Ketac molar was placed for one month before definitive adhesive restoration Receives: Procedure: Restoration |
| Non ITR group | Active comparator | In NON-ITR group, cavity preparation was similar to ITR group, but definitive restoration was done in the same visit Receives: Procedure: Restoration |
What is being measured
The primary outcome is the main question the study is designed to answer.
clinical success
Success was defined as absence of signs and symptoms of irreversible pulpitis (spontaneous pain, fistula and swelling), positive response to pulp sensibility tests.
Measured: 18 months
radiographic success
Absence of periapical alterations (radiolucency at furcal or periapical region, calcification). Pretreatment pulpal diagnosis was considered successful when teeth treated with or without ITR were diagnosed as vital and radiographic signs and symptoms of failure developed.
Measured: 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 May 2017
- Study start20 May 2015
- Primary completion30 Nov 2016
- Study completion30 Nov 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for PulpitisStudies of the same condition, open and under way.
- More trials run by Postgraduate Institute of Dental Sciences RohtakThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 146 participants (actual)
Sponsor and investigators
- Lead sponsor
- Postgraduate Institute of Dental Sciences Rohtak
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Sanjay Tewari, Postgraduate Institute of Dental Sciences Rohtak
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03168620
- Sponsor's protocol ID
- Monikakhokhar
- Status last verified
- May 2017
- First submitted
- 23 May 2017
- Last updated
- 30 May 2017
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 30 May 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Effect of Glass Ionomer Cement as an Interim Restoration in Diagnosis of Pulpal Status in Permanent Teeth: A Prospective Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT03168620
- Acronym / sponsor ID
- Monikakhokhar
- Conditions
- Pulpitis
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 146 participants (actual)
- Lead sponsor
- Postgraduate Institute of Dental Sciences RohtakUniversity, hospital or other
- Study start
- 20 May 2015 (actual)
- Primary completion
- 30 Nov 2016 (actual)
- Study completion
- 30 Nov 2016 (actual)
- First posted
- 30 May 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Aim: To evaluate whether glass ionomer interim therapeutic restoration (ITR) in asymptomatic teeth with deep cavities can help in determining the pulp status. Methodology: 146 mandibular molars with deep carious lesion having positive response to pulp sensitivity were randomly allocated to two study groups (75-ITR, 71- NON-ITR group). In the first group after partial caries removal(PCR), interim therapeutic restoration of glass ionomer cement (GIC) Ketac molar was placed for one month before definitive adhesive restoration. In NON-ITR group, cavity preparation was similar to ITR group, but definitive restoration was done in the same visit. Two examiners evaluated the clinical and radiographic outcomes for 18 months. Success was defined as absence of signs and symptoms of irreversible pulpitis and absence of periapical alterations.
Detailed description
Introduction Preservation of pulp vitality while managing the deep carious lesions is often a great challenge and requires procedures like pulp capping and pulpotomy collectively termed as vital pulp therapy (VPT). Such treatment involves elimination of bacteria from pulp dentine complex and establishing an environment that will prevent any future bacterial contamination and improves survival prognosis. Management of deep carious lesions in recent years has changed from complete caries removal to partial caries removal. Partial caries removal has gained importance due to reduction in pulpal exposures, less postoperative complications, more preservation and maintenance of pulp tissue .
The important concern during VPT is accurate assessment of pulpal status. Methods to determine pulpal vitality include patient history, signs and symptoms, radiographs and pulp sensibility tests. One of the hallmarks of pulpal diagnosis is that it is difficult and has a high rate of inaccuracy. Pain on cold and hot stimuli cannot be considered as a reliable reference for making a treatment decision. Also insufficient evidence was found to determine the diagnostic accuracy of symptoms, signs, and diagnostic tests to assess the pulp status.
Studies using visual and histological inspection of exposed pulp to examine status of pulp reported marked variation in sensitivity of cold and electric pulp test from 0 .21 to 0.94, with relatively less variation in specificity from 0.73 to 0 .96.Sensitivity decreased to 67% when the spectrum of the disease was altered i.e. when asymptomatic teeth with deep carious lesions were included . Diagnosis of pulp status is often easy when there is a clear distinction between healthy and necrosed pulp however it is more difficult in asymptomatic teeth with deep carious lesions.
Recently, Coll et al. proposed that glass ionomer cement (GIC) as interim therapeutic restoration (ITR) improved pulpal diagnosis and VPT outcomes while interpreting diagnostic assessment based on clinical pulp therapy success. Vij et al. reported that GIC temporization for 1-3 months increased success of the subsequent VPT from 79% to 92% .However; both of the studies were retrospective and were in deciduous teeth.
No prospective clinical study has so far been conducted in permanent teeth that demonstrate the effectiveness of GIC and other adhesive restoration materials in determining the pulpal status. Aim of this double blinded randomized controlled trial was to assess the effectiveness of GIC interim restoration in determining the pulpal status of asymptomatic teeth with deep carious lesions. Null hypothesis was that GIC as ITR does not improve the clinician's diagnostic ability to determine the correct pulp clinical diagnosis and does not improve the treatment outcomes in vital pulp therapy.
Material and Methods:
Case Selection This prospective randomized clinical trial was conducted at the Department of Conservative Dentistry and Endodontics, Post Graduate Institute of Dental Sciences, Rohtak, India. The study protocol was approved by the Ethical Committee (PGIDS/IEC/2015/64) of the Post Graduate Institute of Dental Sciences. A total of 146 patients were included with an age range of 15-54 years. The inclusion criteria for the study were: 1) mature permanent mandibular molars having deep carious lesions involving half or more of the dentine detected by radiographic examination, 2) pulp sensibility confirmed using the electric pulp test (Digitest D626D; Parkell Electronics, New York, NY) and the cold test (Endo frost, Coltene, Whaledent), 3) absence of apical and furcal radiolucency determined by radiographic examination, 4) absence of clinical symptoms of irreversible symptoms, fistula, swelling and abnormal tooth mobility. Clinical diagnosis of vital pulp was made by the chief supervisor (Sanjay Tewari) on the basis of radiographic and clinical examination and the pulp sensibility tests. Patients were excluded if they presented with signs and symptoms of irreversible pulpitis, had negative response to vitality tests before or after ITR, diabetic, immunocompromised, pregnant, or had a positive history of antibiotic use in past one month or required antibiotic prophylaxis. Informed consent explaining benefits and risks of treatment was taken from patients before participation in the trial.
Sample Size Calculation and Randomization The sample size calculation was done on the basis of difference in the percentage of success of vital pulp therapy using GIC (98%) versus non-GIC group (75%) (12) α=5% with a power of 90%. This indicated the need for 48 restorations per treatment group. Given an expected attrition rate of 20%, 60 teeth were included in each treatment group. Randomization was developed to eliminate any bias on the part of the investigators and to equalize the number of patients between the 2 treatment groups. Using an equal proportion randomization allocation ratio, one of the investigators (M.J) created envelopes containing concealed assignment codes that were assigned sequentially to eligible patients.
Clinical Procedure The procedure was performed under local anesthesia and rubber dam isolation. Carious tissue from the lateral walls and dentinoenamel junction was removed completely by using low-speed metal burs and/or hand excavator. Superficial necrotic dentin was removed from the pulpal and axial wall using low speed round bur. A layer of soft, wet carious dentin was left adjacent to pulpal wall. The cavity was cleaned with distilled water and dried with sterile filter paper. In group ITR, the cavity was filled with GIC ( Ketac Molar (3M ESPE, St. Paul, Minn., USA).Cavity was reopened after 1 months in asymptomatic patients , restoration was removed completely ,base of resin modified glass ionomer cement(RMGIC) (Fuji Lining LC;GC,Tokyo,Japan)was applied and cavity was restored with resin composite(Tetric N-Ceram;Ivoclar Vivadent) according to manufacturer instructions.
In NON-ITR group, cavity preparation was done similar to ITR group, after partial caries excavation ,base of RMGIC (Fuji Lining LC;GC,Tokyo,Japan) was applied and all cavities were restored with resin composite(Tetric N-Ceram;Ivoclar Vivadent) according to manufacturer instructions.
Outcome Assessment Two blinded examiners assessed the clinical and radiographic outcomes of test and control treatments at 1, 3, 6, 12, 18 months after treatment. Success was defined as absence of signs and symptoms of irreversible pulpitis (spontaneous pain, fistula and swelling), positive response to pulp sensibility tests and absence of periapical alterations (radiolucency at furcal or periapical region, calcification) (combined outcome). Pretreatment pulpal diagnosis was considered successful when teeth treated with or without ITR were diagnosed as vital and none of clinical and radiographic signs and symptoms of failure developed during 18 month follow up.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ITR group | Active comparator | Procedure: RestorationIn ITR group after partial caries removal(PCR), interim therapeutic restoration of glass ionomer cement (GIC) Ketac molar was placed for one month before definitive adhesive restoration |
| Non ITR group | Active comparator | Procedure: RestorationIn NON-ITR group, cavity preparation was similar to ITR group, but definitive restoration was done in the same visit |
Who may qualify
- Ages
- 15 to 54 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (10 listed)
- mature permanent mandibular molars having deep carious lesions involving half or more of the dentine detected by radiographic examination,
- pulp sensibility confirmed using the electric pulp test (Digitest D626D; Parkell Electronics, New York, NY) and the cold test (Endo frost, Coltene, Whaledent),
- absence of apical and furcal radiolucency determined by radiographic examination,
- absence of clinical symptoms of irreversible symptoms, fistula, swelling and abnormal tooth mobility.
- Clinical diagnosis of vital pulp was made on the basis of radiographic and clinical examination and the pulp sensibility tests.
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| RestorationAlso: Filling | Procedure or surgery | ITR group, Non ITR group |
Primary outcome
clinical success
Time frame: 18 months
Success was defined as absence of signs and symptoms of irreversible pulpitis (spontaneous pain, fistula and swelling), positive response to pulp sensibility tests.
radiographic success
Time frame: 18 months
Absence of periapical alterations (radiolucency at furcal or periapical region, calcification). Pretreatment pulpal diagnosis was considered successful when teeth treated with or without ITR were diagnosed as vital and radiographic signs and symptoms of failure developed.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 May 2017.
- Individual participant dataSharing planned: Yes
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
A study testing Restoration in people with Pulpitis, run by Postgraduate Institute of Dental Sciences Rohtak.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 30 May 2017. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
clinical success (time frame: 18 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 May 2017.