MedPath

To compare the analgesic effect of buprenorphine through epidural and trandermal routes in patients undergoing hysterectomy.

Phase 4
Conditions
Health Condition 1: null- Undergoing Hysterectomy
Registration Number
CTRI/2018/05/013594
Lead Sponsor
Anju Krishnan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a)Age between20 and 65 years.

American Society of Anaesthesiologists ASA I OR II.

Expected hospital stay after intervention atleast for 72 hrs.

Weight 45kg -65kg.

Exclusion Criteria

Any chronic pain syndromes.

Chronic obstructive pulmonary disease.

Any history of hypersensitivity to opioids or patch additives.

Obstructive sleep apnoea.

Psychiatric disorders which impact on appropriate data collection.

Surgeries lasting for more than 2 hours.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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