The efficacy of laparoscopic Transversus Abdominis Block on pain and side-effects reduction of surgery

Evaluating the efficacy of laparoscopic Transversus Abdominis Block on pain and side-effects reduction in laparoscopic bariatric surgeries in Imam Khomeini hospital complex in 2020-2021

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20201007048962N1

Enrollment

Registered

2020-12-17

Start date

2020-11-21

Completion date

Unknown

Last updated

2021-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Laparoscopic bariatric surgery. Condition 2: postprocedural pain. Bariatric surgery status Other acute postprocedural pain

Interventions

Intervention 1: Intervention group: The Braun Stimuplex Ainsulated needle will enter the skin from the mid-axillary line between the iliac crest and the rib margin. The needle is advanced to the dista

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Laparoscopic bariatric surgery

Exclusion criteria

Exclusion criteria: No patients consent for participation in the study Patients whose surgery becomes open or an unusual complication occurs.

Design outcomes

Primary

Measure	Time frame
Pain score. Timepoint: 6, 24 and 48 hours post surgery. Method of measurement: Visual Analogue Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadadi Bahri

Tehran University of Medical Sciences

m.bahri@abzums.ir??? ?????

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026