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Crown LengtheningNCT07653802

Comparison of Er:YAG Assisted Laser Crown Lengthening Against Surgical Crown Lengthening

A study testing conventional surgical crown lengthening by opening envelop flap and crown lengthening using Er:YAG Laser in people with Crown Lengthening and Crown Lengthening Procedure With Ostectomy, run by Gulf Medical University at 1 site in United Arab Emirates.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Crown lengthening is a clinical procedure that involves reshaping the gingiva, and sometimes bone, in order to expose more of tooth's structure. The procedures is performed for both functional and aesthetic reasons. Read more about this study

Who is it for?
Ages 20 to 70 yearsHealthy volunteers can take part
What is being tested?
conventional surgical crown lengthening by opening envelop flap and crown lengthening using Er:YAG Laser
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
26 participants
Where
1 siteUnited Arab Emirates
Study dates
1 Jul 2025to 30 Sep 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 20 to 70 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Teeth indicated for crown lengthening procedure either in the maxillary or mandibular arch.
  • Patients in the age group of 18-75 years.

Who cannot join

  • Patients with uncontrolled diabetes mellitus. Uncontrolled diabetes mellitus diagnosed with HbA1C ≥ 7% will be an exclusion criterion.
  • Smokers (considered as smoking ≥ 10 cigarettes/day)
  • Pregnant women
  • Patients with uncontrolled systemic diseases that may affect the healing of soft and hard tissues of the periodontium will be excluded.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Nesma Shemais contact

0529961988

dr.nesma@gmu.ac.ae

United Arab Emirates1 site, 1 recruiting
  • Gulf Medical University

    Ajman, Ajman Emirate, 00000

    Nesma Shemais, PhD, 0529961988, dr.nesma@gmu.ac.ae

    Recruiting

Other trials in United Arab Emirates

About this study

Official title: Comparison of Er:YAG Assisted Laser Crown Lengthening Against Surgical Crown Lengthening: a Longitudinal Study.

Crown lengthening is a clinical procedure that involves reshaping the gingiva, and sometimes bone, in order to expose more of tooth's structure. The procedures is performed for both functional and aesthetic reasons. In certain instances, this procedure is performed to This procedure is commonly performed for both functional and aesthetic reasons, such as to prepare a tooth for a crown or to enhance the appearance of a smile. Traditional crown lengthening techniques typically involve surgical methods that can be invasive, leading to extended recovery times and postoperative discomfort in this study we compare traditional versus the laser aided crown lengthening to compare the periodontal parameters in both cases.

Read the detailed description

Crown lengthening is a clinical procedure that involves reshaping the gingiva, and sometimes bone, in order to expose more of tooth's structure. The procedures is performed for both functional and aesthetic reasons. In certain instances, this procedure is performed to This procedure is commonly performed for both functional and aesthetic reasons, such as to prepare a tooth for a crown or to enhance the appearance of a smile. Traditional crown lengthening techniques typically involve surgical methods that can be invasive, leading to extended recovery times and postoperative discomfort in this study we compare traditional versus the laser aided crown lengthening to compare the periodontal parameters in both cases.

Laser technology and minimally invasive therapy have become increasingly prominent in various dental fields. The erbium:YAG laser, the newest type, can be used on both soft and hard tissues. This study evaluates the periodontal outcomes of a flapless crown lengthening procedure using the erbium:YAG laser in comparison to traditional methods.

Crown lengthening aims to obtain a larger crown surface by surgical means either by gingivectomy or by recontouring of the cortical bone. The obtained increased crown surface can be used to build crowns.

Conventional surgical techniques involve incisions, elevation of flap and osteoplasty. Subsequently, the flaps are approximated and sutured.

LASER stands for Light amplification by stimulated emission of radiation. Several lasers are used in dentistry including soft and hard tissue lasers. Soft tissue lasers including diode lasers are used to incise the soft tissue, whereas lasers including Er:YAG lasers hard tissue lasers can be used to Er:YAG lasers are known to have good cutting and coagulation abilities on soft tissues.(1) Upon use in soft tissues the laser provides good coagulation resulting in bleeding control. The laser is capable of Lasers offer significant advantages including reduced bacteraemia, reduced post operative discomfort, improved bleeding control and quicker healing. The comfort of avoiding a surgical procedure is an added advantage which may make the patient less concerned about opting for treatment options.

Being tested
conventional surgical crown lengthening by opening envelop flap, crown lengthening using Er:YAG Laser
Keywords
crown lengthening

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • conventional surgical crown lengthening by opening envelop flapProcedure or surgery

    Bevel incision with number 15 blades is place on the margin following with sulcular incision and excess gingival tissues are removed using Gracey currets .in case if any granulation tissues are seen it should be removed and washed with saline.

    Following with bone recontouring and reshaping after periosteal elevator is used to expose the underlying bone. fissure burs or coarse diamond stones are used until thing bone tissues are left over the root and rest can be removed with scaler to prevent damage to the tooth.

    Resorbable sutures are place after the surgery and the case is followed up for 3 months period.

    In the case of conventional surgical crown lengthening, after delivering the local anesthetic solution to the surgical area, soft tissue recontouring starts. This procedure, which involves excising the soft tissue with a gingivectomy, is typically done to improve aesthetics or create more space for better restoration seating. The gingival border is typically 1 mm coronal to the CEJ.

  • crown lengthening using Er:YAG LaserProcedure or surgery

    Er:YAG laser is used for both soft and hard tissue recontouring according to the manufacturer's guidelines. In the case of gingivectomy and soft tissue recontouring, 4x17mm, 0.6x17mm, and 1.3x17mm tips are used, and the soft tissue mode is selected on the device screen, which sets the device parameters to 100mJ x 20Hz. The tip is in direct contact with the soft tissue until the desired soft tissue level is achieved. For bone contouring, the hard tissue option is selected on the device's screen, setting the parameters to 150mJ x 20Hz. A non-contact approach is used to reshape the underlying bone.

Study groups in NCT07653802
Study groupRoleWhat they receive
crown lengthening using Er:YAG LaserExperimentalEr:YAG laser is used for both soft and hard tissue recontouring according to the manufacturer's guidelines. In the case of gingivectomy and soft tissue recontouring, 4x17mm, 0.6x17mm, and 1.3x17mm tips are used, and the soft tissue mode is selected on the device screen, which sets the device parameters to 100mJ x 20Hz. The tip is in direct contact with the soft tissue until the desired soft tissue level is achieved. For bone contouring, the hard tissue option is selected on the device's screen, setting the parameters to 150mJ x 20Hz. A non-contact approach is used to reshape the underlying bone.
Receives: Procedure: crown lengthening using Er:YAG Laser
: conventional surgical crown lengthening by opening envelop flapActive comparatorBevel incision with number 15 blades is place on the margin following with sulcular incision and excess gingival tissues are removed using Gracey currets .in case if any granulation tissues are seen it should be removed and washed with saline. Following with bone recontouring and reshaping after periosteal elevator is used to expose the underlying bone. fissure burs or coarse diamond stones are used until thing bone tissues are left over the root and rest can be removed with scaler to prevent damage to the tooth. Resorbable sutures are place after the surgery and the case is followed up for 3 months period. In the case of conventional surgical crown lengthening, after delivering the local anesthetic solution to the surgical area, soft tissue recontouring starts. This procedure, which involves excising the soft tissue with a gingivectomy, is typically done to improve aesthetics or create more space for better restoration seating. The gingival border is typically 1 mm coronal to the CEJ
Receives: Procedure: conventional surgical crown lengthening by opening envelop flap

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postoperative Pain

    VAS 0-10

    Measured: baseline, 3 days

  2. Postoperative pain

    VAS scale 0-10

    Measured: baseline 3 days

Secondary outcomes (2)
  1. Probing depth

    Measured: baseline, 3 months , 6 months

  2. patient satisfaction VAS

    VAS 0-10

    Measured: baseline, 3 days , 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Jun 2026
  2. Study start1 Jul 2025
  3. Primary completion1 Sep 2026 (estimated)
  4. Study completion30 Sep 2026 (estimated)

Resources

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
26 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07653802
Sponsor's protocol ID
Ali-MDSperio
Status last verified
Jun 2026
First submitted
10 Jun 2026
Last updated
17 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing conventional surgical crown lengthening by opening envelop flap and crown lengthening using Er:YAG Laser in people with Crown Lengthening and Crown Lengthening Procedure With Ostectomy, run by Gulf Medical University at 1 site in United Arab Emirates.

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 2 inclusion and 4 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: looking for participants now, as of the sponsor's last update on 17 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Arab Emirates. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Nesma Shemais (0529961988, dr.nesma@gmu.ac.ae), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postoperative Pain (time frame: baseline, 3 days). 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 17 Jun 2026.

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Clinical Trial NCT07653802 | AzTrials