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Does the infiltration of Levobupivacaine into the rectus abdominus muscle ( Rectus Sheath Block) improve post-operative analgesia following open gastric bypass for morbid obesity? - Obesity surgery research

Phase 1
Active, not recruiting
Conditions
Morbid Obesity.
Registration Number
EUCTR2005-000803-32-GB
Lead Sponsor
eeds Teaching Hospitals NHS Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Recruiting
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Patients who will be invited to participate in the study will be English-speaking Euro-Caucasian women between 18 and 60 years of age with a body mass index between 35 and 55. All Patients will be scheduled to undergo bariatric surgery with Roux loop formation for morbid obesity. Surgery will be performed at SJUH and the Leeds BUPA Hospital between April 2005 and December 2005.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1.Patient refusal.
2.Prior enrolment in an alternative investigation.
3.Age <18 or >60 years.
4.Body mass index >55
5.Allergy or intolerance to any of the study drugs including non-steroidal anti-inflammatories. This includes diabetic patients with proteinuria in whom NSAIDS are relatively contraindicated.
6.Inability to understand or use the VAS for post-operative assessment.
7.Pregnancy and lactation.
8.Previous upper abdominal surgery.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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