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A clinical trial to compare the analgesic effect of three modalities, epidural block , TAP block and combined parenteral diclofenac and tramodol in patients undergoing total abdominal hysterectomy.

Quality of recovery from general anaesthesia after total abdominal hysterectomy.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/06/001823
Enrollment
60
Registered
2011-06-21
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- quality of recovery in ASA I-II patients undergoing total abdominal hystercetomy

Interventions

Intervention1: transversus abdominis plane block: single shot blind technique, bilateral 15 ml of 0.25% bupivacaine Intervention2: epidural block: postoperatively 0.125% bupivacaine 8cc- 5 doses Contr

Sponsors

post graduate institute of medical education and research chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA I-II patients 2.age 18-65 years 3.total abdominal hysterectomy +/- bilateral salpingo-oophorectomy

Exclusion criteria

Exclusion criteria: inability to cooperate BMI >30 ASA grade > III(moderate to severe heart or lung disease) history of drug or alcohol abuse complaint of chronic pain/daily intake of analgesics contraindications to NSAIDs/insertion of epidural catheter undergoing omentectomy,lymph node dissection or radical hysterectomy

Design outcomes

Primary

MeasureTime frame
quality of recovery as assessed by QOR-40Timepoint: postoperative at 24,48,72 hours—

Secondary

MeasureTime frame
postoperative pain scores as assessed by NRS and rescue analgesic(morphine) requirementTimepoint: postop at 0min,30 min, 60 min, 90 min, 2 hours, 4 hours ,6hours, 12 hours,18hours, 24hours—

Countries

India

Contacts

Public Contactdr neelam aggarwal

postgraduate institute of medical education and research

tjpreethy@rediffmail.com9914209530

Outcome results

None listed

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