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Comparison of efficacy of a local anaesthetic agent with a steroid in providing pain relief in a abdominal plane block after lower abdominal operations.

Comparative evaluation of ropivacaine and ropivacaine with dexamethasone in transverse abdominis plane block for lower abdominal surgeries.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008880
Enrollment
70
Registered
2017-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients who are being posted for elective lower abdomen surgeries belonging to ASA physical status I and II

Interventions

Intervention1: Ropivacaine with saline: Ropivacaine 0.25% 20ml mixed with 2 ml saline once at the end of surgery in Transverse abdominal plane block Intervention2: Transverse abdominis plane block: Ul

Sponsors

Shri Sathya Sai Medical College and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of both the sexes weighing between 40 - 100 kgs of physical status ASA I and II undergoing elective lower abdominal surgery under general anaesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients refusal for the transverse abdominis plane block 2. Patients belonging to ASA III IV and V physical status 3. Patients allergic to local anaesthetics and dexamethasone 4. Presence of infection at the needle insertion site over the abdomen 5. Patients currently using analgesics or who had current acute or chronic pain

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study would be to evaluate the effects of dexamethasone on the time to the first request for additional analgesics in minutes after the surgeryTimepoint: In minutes for first 24 hours after the surgery

Secondary

MeasureTime frame
1 The pain scores (NPIS scale 0-10) at rest 2 Total analgesic consumption (Morphine in mg) 3 Occurrence of nausea/vomitingTimepoint: Would be recorded for the first 24 hours after the surgery

Countries

India

Contacts

Public ContactDr N Gnanasekar

Shri Sathya Sai Medical College and Research Institute

matmon_3641@hotmail.com9884906893

Outcome results

None listed

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