Overview

The Analgesic Effect of Transversus Abdominis Plane (TAP) Block Following Radical Prostatectomy

Status:
Completed
Trial end date:
2012-02-01
Target enrollment:
0
Participant gender:
Male
Summary
This study is conducted to evaluate different analgesic treatments effect following operation where the prostate gland is surgically removed. The different treatments the investigators wish to investigate is: 1. Transversus Abdominis Plane (TAP) block. The TAP block is a rather new method, where a local anaesthetic is deposited between the two inner abdominal muscles. Between these muscles, the nerves that innervates the anterior part of the abdominal wall is situated. 2. Wound infiltration In this method you deposit a local anaesthetic in the edges of the wound. 3. Placebo No active local treatment is given. All patients who wish to participate will be allocated to one of three different treatment groups. Group 1: Will receive TAP block with a local anaesthetic and wound infiltration with saline. Group 2: Will receive wound infiltration with a local anaesthetic and TAP block with saline. Group 3: Will receive TAP block with saline and wound infiltration with saline. Beside this local treatment all patients will be given systemic Paracetamol (tablet) and Ibuprofen (tablet). In addition all patients will be given a pump containing morphine. The pump is connected to a button which the patient can activate when they experience pain. This enables the patient to control how much morphine he needs, following the operation. The hypothesis is that the TAP block is superior in reducing pain and thereby reducing morphine consumption compared to wound infiltration and placebo.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Rigshospitalet, Denmark
Treatments:
Analgesics
Ropivacaine
Criteria
Inclusion Criteria:

- BMI > 18 and < 35

- Patients who have given their informed consent and have fully understood the nature
and limitations of the study

- Patient who is planned for radical prostatectomy

Exclusion Criteria:

- Not able to cooperate to complete the study

- Is not able to speak and understand danish

- Allergy towards the drugs which is used in the study

- Daily use of strong opioids

- Infection at the injection area