PengblockNCT06995079
Comparıson Of The Effects Of Perıcapsulary Nerve Group Block (Peng Block) And Lumbar Erector Spına Plan Block (Lesp Block) On Postoperatıve Opıoıd Consumptıon
A study testing Postoperative pain assessment of patients who underwent block in people with Pengblock and over65years, run by Sakarya University.
Trial summary
The aim is to demonstrate that lumbar ESP block provides more effective postoperative analgesia than PENG block in geriatric patients with hip fractures, and reduces postoperative opioid consumption more than PENG block Read more about this study
- Who is it for?
- Ages 65 years and older
- Conditions the study is for
- Pengblock, over65years, Lumbar Erector Spinae Plane Block
- What is being tested?
- Postoperative pain assessment of patients who underwent block
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 70 participants
- Where
- No sites listed yet
- Study dates
- Jun 2025to Jan 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 65 years and older
- All sexes
- No healthy volunteers
- Older adult
Who may be able to join
- patients with hip fractures
- over 65 years old
Who cannot join
- long-term surgery
- Patients who do not want regional anesthesia
- bleeding disorder disease
- wound in the operation area
About this study
Official title: Comparison of the Effects of Pericapsular Nerve Group Block (Peng Block) and Lumbar Erector Spinae Plane Block (Lesp Block) on Postoperative Opioid Consumption in Geriatric Patients Undergoing Hip Fracture Surgery
The aim is to demonstrate that lumbar ESP block provides more effective postoperative analgesia than PENG block in geriatric patients with hip fractures, and reduces postoperative opioid consumption more than PENG block
- Conditions
- Pengblock, over65years, Lumbar Erector Spinae Plane Block, Hipfracture
- Being tested
- Postoperative pain assessment of patients who underwent block
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Postoperative pain assessment of patients who underwent blockProcedure or surgery
Postoperative pain assessment of patients who underwent block
| Study group | Role | What they receive |
|---|---|---|
| pericapsular nerve group block (peng block) | Experimental | The patient will first be taken to the block room in the operating room.In this group, patients will be given a Peng block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed Receives: Procedure: Postoperative pain assessment of patients who underwent block |
| lumbar erector spinae plane block(lesp block) | Experimental | The patient will first be taken to the block room in the operating room.In this group, patients will be given a lumbar erector spinae plane block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed Receives: Procedure: Postoperative pain assessment of patients who underwent block |
What is being measured
The primary outcome is the main question the study is designed to answer.
postoperative pain
To evaluate postoperative pain after two different block applications in patients undergoing hip fracture surgery.Evaluation of patients' postoperative 30th minute, 2nd hour, 6th hour, 12th hour and 24th hour verbal analog scores.To examine the total fentanyl consumption, acetaminophen consumption, and nonsteroidal anti-inflammatory drug consumption of patients in the postoperative 24 hours.
Measured: 6 month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 May 2025
- Study startJun 2025 (estimated)
- Primary completionNov 2025 (estimated)
- Study completionJan 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for PengblockStudies of the same condition, open and under way.
- More trials run by Sakarya UniversityThe 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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 70 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Sakarya University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06995079
- Sponsor's protocol ID
- PENGVSLESP
- Status last verified
- May 2025
- First submitted
- 7 May 2025
- Last updated
- 29 May 2025
- 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 29 May 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of the Effects of Pericapsular Nerve Group Block (Peng Block) and Lumbar Erector Spinae Plane Block (Lesp Block) on Postoperative Opioid Consumption in Geriatric Patients Undergoing Hip Fracture Surgery
- ClinicalTrials.gov ID
- NCT06995079
- Acronym / sponsor ID
- PENGVSLESP
- Conditions
- Pengblock, over65years, Lumbar Erector Spinae Plane Block, Hipfracture
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 70 participants (estimated)
- Lead sponsor
- Sakarya UniversityUniversity, hospital or other
- Study start
- Jun 2025 (estimated)
- Primary completion
- Nov 2025 (estimated)
- Study completion
- Jan 2026 (estimated)
- First posted
- 29 May 2025 (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.
The aim is to demonstrate that lumbar ESP block provides more effective postoperative analgesia than PENG block in geriatric patients with hip fractures, and reduces postoperative opioid consumption more than PENG block
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| pericapsular nerve group block (peng block) | Experimental | Procedure: Postoperative pain assessment of patients who underwent blockThe patient will first be taken to the block room in the operating room.In this group, patients will be given a Peng block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed |
| lumbar erector spinae plane block(lesp block) | Experimental | Procedure: Postoperative pain assessment of patients who underwent blockThe patient will first be taken to the block room in the operating room.In this group, patients will be given a lumbar erector spinae plane block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed |
Who may qualify
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Older adult
Key inclusion criteria (2 listed)
- patients with hip fractures
- over 65 years old
Key exclusion criteria (4 listed)
- long-term surgery
- Patients who do not want regional anesthesia
- bleeding disorder disease
- wound in the operation area
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 |
|---|---|---|
| Postoperative pain assessment of patients who underwent blockPostoperative pain assessment of patients who underwent block | Procedure or surgery | lumbar erector spinae plane block(lesp block), pericapsular nerve group block (peng block) |
Primary outcome
postoperative pain
Time frame: 6 month
To evaluate postoperative pain after two different block applications in patients undergoing hip fracture surgery.Evaluation of patients' postoperative 30th minute, 2nd hour, 6th hour, 12th hour and 24th hour verbal analog scores.To examine the total fentanyl consumption, acetaminophen consumption, and nonsteroidal anti-inflammatory drug consumption of patients in the postoperative 24 hours.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 May 2025.
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.
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 Postoperative pain assessment of patients who underwent block in people with Pengblock and over65years, run by Sakarya University.
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: opening soon, as of the sponsor's last update on 29 May 2025. 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?
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?
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?
postoperative pain (time frame: 6 month). 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 29 May 2025; AzTrials last refreshed its copy on 7 Nov 2026.