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The comparison of pain relieving efficay of subcostal transversus abdominis plane (TAP) catheters with epidural infusion in patients undergoing surgery on their upper abdomen

Comparison of analgesic efficacy of oblique subcostal transversus abdominis plane (TAP) catheters with epidural analgesia in patients undergoing upper abdominal surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN08486065
Enrollment
66
Registered
2009-11-23
Start date
2009-07-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Upper Abdominal Surgery Surgery

Interventions

Please note that as of 05/07/10 this trial has been completed. The original anticipated end date was 30/12/10. 1. Ultrasound guided insertion of oblique subcostal transversus abdominis plane (TAP) ca

Sponsors

University Hospitals of Leicester NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients aged over 18 years who are scheduled for elective upper abdominal surgery involving incisions with the lower end of the incision at or above thoracic T 10 dermatome 1. Bisubcostal incision 2. Unisubcostal incision 3. Upper midline incision 4. Nephrectomy incision

Exclusion criteria

Exclusion criteria: 1. Lack of consent including from those patients who lack mental capacity to give informed consent 2. Patients with history of drug allergy to bupivacaine 3. Patients with history of chronic pain conditions: defined as patients with history of pain for above 3 months and who consume regular analgesics for their chronic pain 4. American Society of Anesthesiologists (ASA) Class 4 and 5 5. Upper abdominal surgery where the lower end of the incision extends below T 10 dermatome

Design outcomes

Primary

MeasureTime frame
The Visual Analogue Scale (VAS) scores at rest and on coughing before surgery and at the 9 time periods after surgery.

Secondary

MeasureTime frame
1. Post operative categorical nausea scores before surgery and at the 9 time periods after surgery (none = 0; mild = 1; moderate = 2; severe = 3). 2. Patient satisfaction with postoperative analgesia at 24 h, 48 h and 72 h 3. Any complications with either epidural catheters or TAP catheters during first 72 hours after surgery

Countries

United Kingdom

Outcome results

None listed

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