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Post operative pain control after abdominal gynaecological surgery using pump-releasing local anaesthetic for 24 hours continuously

Post operative pain control after abdominal gynaecological surgery using pump-releasing local anaesthetic for 24 hours continuously: a prospective, double-blind, randomised, placebo-controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN28558391
Enrollment
80
Registered
2004-09-30
Start date
2002-03-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Signs and Symptoms: Pain Signs and Symptoms

Interventions

The surgery will be performed under general anaesthetic induced with fentanyl and propofol. Vecuronium will be administered to facilitate tracheal intubation and for neuromuscular block during surgery

Sponsors

Department of Health
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 80 women aged 30 to 70 years undergoing elective gynaecological surgery performed through a transverse incision in the lower abdomen.

Exclusion criteria

Exclusion criteria: 1. Patients with a known allergy to morphine, fentanyl, propofol, vecuronium, diclofenac or marcain. 2. Regular medication with opioids for the last 6 months. 3. Body mass index (BMI) greater or equal to 32. 4. Previous major surgery during the last 6 months.

Design outcomes

Primary

MeasureTime frame
1. Post operative pain at 4, 8, 12, 24, 36, 48 and 72 hours while at rest, coughing and mobilising from supine to sitting position in bed, assessed using a 10 point visual analogue scale. 2. Gastric emptying will be recorded on a trial sheet. 3. Opioid consumption will be recorded using the Patient Controlled Analgesia device and included on the trial sheet for 3 days post op.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

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