AnalgesiaNCT05960253
Peroperative Effect of Regional Anesthesia in Hip Surgery
A study testing Pericapsular Nerve Group Block and Lumber Erector Spinae Plane Block in people with Analgesia, run by Ankara City Hospital Bilkent at 1 site in Turkey (Türkiye).
Trial summary
A total of 120 patients scheduled for surgical operation due to hip fracture were divided into two randomized groups. The first group received pericapsular nerve group (PENG) block, while the second group received lumbar erector spinae plane (L-ESP) block prior to the surgery. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Analgesia
- What is being tested?
- Pericapsular Nerve Group Block and Lumber Erector Spinae Plane Block
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 20 Aug 2023to 1 Dec 2023
- 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- American Society of Anesthesiologists(ASA) 2-3 patients undergoing surgery due to hip fracture.
Who cannot join
- Patients in whom regional anesthesia is contraindicated.
- Patients who are unable to communicate.
- Patients with a known allergy to local anesthetics.
- Patients with organ failure.
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site, 1 recruiting
- Recruiting
Ankara City Hospital
Ankara, 06800
Kevser Yamen, MD, +905544669049, kevser.yamen@gmail.com
About this study
Official title: Comparison of the Peroperative Efficacy of Pericapsular Nerve Group Block and Lumbar Erector Spina Plan Block Applied Preoperatively in Patients Undergoing Hip Fracture Operation
A total of 120 patients scheduled for surgical operation due to hip fracture were divided into two randomized groups. The first group received pericapsular nerve group (PENG) block, while the second group received lumbar erector spinae plane (L-ESP) block prior to the surgery. Subsequently, all patients were positioned in the lateral decubitus position before spinal anesthesia and compared in terms of anesthesia effectiveness through pain scores.
- Conditions
- Analgesia
- Being tested
- Pericapsular Nerve Group Block, Lumber Erector Spinae Plane Block
- Medical subject headings
- Agnosia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pericapsular Nerve Group BlockProcedure or surgery
1st group to be applied PENG block
Lumber Erector Spinae Plane BlockProcedure or surgery
2nd group to be applied Lumber ESP block
| Study group | Role | What they receive |
|---|---|---|
| PENG block group | Active comparator | Not described Receives: Procedure: Pericapsular Nerve Group Block |
| L-ESP group | Experimental | Not described Receives: Procedure: Lumber Erector Spinae Plane Block |
What is being measured
The primary outcome is the main question the study is designed to answer.
Analgesia
Pain measurement via Visual Analog Scale (VAS) scores
Measured: 30 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Jul 2023
- Study start20 Aug 2023
- Primary completion1 Sep 2023
- Study completion1 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AnalgesiaStudies of the same condition, open and under way.
- More trials run by Ankara City Hospital BilkentThe 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
- Supportive care
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ankara City Hospital Bilkent
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Levent Öztürk, Ankara City Hospital Bilkent
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05960253
- Sponsor's protocol ID
- hip surgery
- Status last verified
- Nov 2023
- First submitted
- 18 Jul 2023
- Last updated
- 28 Nov 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Nov 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of the Peroperative Efficacy of Pericapsular Nerve Group Block and Lumbar Erector Spina Plan Block Applied Preoperatively in Patients Undergoing Hip Fracture Operation
- ClinicalTrials.gov ID
- NCT05960253
- Acronym / sponsor ID
- hip surgery
- Conditions
- Analgesia
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- Ankara City Hospital BilkentUniversity, hospital or other
- Study start
- 20 Aug 2023 (actual)
- Primary completion
- 1 Sep 2023 (actual)
- Study completion
- 1 Dec 2023 (estimated)
- First posted
- 25 Jul 2023 (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.
A total of 120 patients scheduled for surgical operation due to hip fracture were divided into two randomized groups. The first group received pericapsular nerve group (PENG) block, while the second group received lumbar erector spinae plane (L-ESP) block prior to the surgery. Subsequently, all patients were positioned in the lateral decubitus position before spinal anesthesia and compared in terms of anesthesia effectiveness through pain scores.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| PENG block group | Active comparator | Procedure: Pericapsular Nerve Group Block |
| L-ESP group | Experimental | Procedure: Lumber Erector Spinae Plane Block |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- American Society of Anesthesiologists(ASA) 2-3 patients undergoing surgery due to hip fracture.
Key exclusion criteria (4 listed)
- Patients in whom regional anesthesia is contraindicated.
- Patients who are unable to communicate.
- Patients with a known allergy to local anesthetics.
- Patients with organ failure.
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 |
|---|---|---|
| Pericapsular Nerve Group Block1st group to be applied PENG block | Procedure or surgery | PENG block group |
| Lumber Erector Spinae Plane Block2nd group to be applied Lumber ESP block | Procedure or surgery | L-ESP group |
Primary outcome
Analgesia
Time frame: 30 minutes
Pain measurement via Visual Analog Scale (VAS) scores
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Nov 2023.
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Pericapsular Nerve Group Block and Lumber Erector Spinae Plane Block in people with Analgesia, run by Ankara City Hospital Bilkent at 1 site in Turkey (Türkiye).
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 1 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: status not confirmed, as of the sponsor's last update on 28 Nov 2023. 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 Turkey (Türkiye). 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Analgesia (time frame: 30 minutes). 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 28 Nov 2023; AzTrials last refreshed its copy on 7 Nov 2026.