CClinicalTrials.gg
Not yet recruitingNCT06925945Updated Apr 17, 2025

Modified Thoracoabdominal Plane Block and Rectus Block Combination

An interventional study of regional anestesia in Visual Analogue Scale, sponsored by Haseki Training and Research Hospital. Not yet recruiting. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-04-17.

Sponsored by Haseki Training and Research Hospital · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 1 month ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The aim of our study was to investigate the effect of the combination of Modified thoracoabdominal plane block (M-TAPA) and rectus sheath block with local infiltration analgesia on postoperative pain scores and opioid use.

02

Conditions studied

  • Visual Analogue Scale
03

In context

Lead sponsor

Haseki Training and Research Hospital is the lead sponsor of 75 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Over 18 years old
  • ASA1-2
  • Laparoscopic cholecystectomy cases

Exclusion criteria

Exclusion Criteria:

  • Bleeding disorders
  • Anticoagulant use
  • Patients with previous nerve damage
  • Lack of patient consent
  • Patients with liver and kidney failure
  • Patients allergic to local anesthetics used
  • Patients with BMI > 35
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Modified thoracoabdominal plane block (M-TAPA) and rectus sheath block

    Modified thoracoabdominal plane block (M-TAPA) and rectus sheath block

    Procedure: regional anestesia

  • Active comparator
    local infiltration analgesia

    local infiltration analgesia

    Procedure: regional anestesia

Interventions

  • Procedureregional anestesia

    Modified thoracoabdominal plane block (M-TAPA) and rectus sheath block with local infiltration analgesia

06

What researchers measure

Primary outcomes

  1. visual analogue scale

    Pain score measured using a 0-10 scale, where 0 = no pain and 10 = worst imaginable pain. Higher scores indicate worse pain.

    Time frame: 4 month

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Gungor H, Ciftci B, Alver S, Golboyu BE, Ozdenkaya Y, Tulgar S. Modified thoracoabdominal nerve block through perichondrial approach (M-TAPA) vs local infiltration for pain management after laparoscopic cholecystectomy surgery: a randomized study. J Anesth. 2023 Apr;37(2):254-260. doi: 10.1007/s00540-022-03158-0. Epub 2022 Dec 28. PubMed 36575362 ↗
  • Erten E, Kara U, Simsek F, Oztas M, Suzer MA, Kamburoglu H, Eskin MB, Senkal S, Cosar A. Modified thoracoabdominal nerves block through perichondrial approach for laparoscopic cholecystectomy. Rev Assoc Med Bras (1992). 2024 Apr 22;70(3):e20230962. doi: 10.1590/1806-9282.20230962. eCollection 2024. PubMed 38655995 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06925945
Lead sponsor
Haseki Training and Research Hospital
Responsible party
Ali Hüseyin Demir (MD, Haseki Training and Research Hospital) — Principal investigator
First posted
Apr 13, 2025
Start date
Apr 10, 2025 (estimated)
Primary completion
Aug 10, 2025 (estimated)
Completion
Aug 15, 2025 (estimated)
Last update
Apr 17, 2025

Study contacts

ALİ HÜSEYİN DEMİR
Contact
alihdemir92@gmail.com
+905062958099

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion