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A study to compare changes in blood sugar levels after addition of 2 different doses of dexamethasone to local anaesthetic for pain relief in patients undergoing caesarean section surgeries

Phase 1
Conditions
Health Condition 1: O82- Encounter for cesarean delivery without indication
Registration Number
CTRI/2023/11/059419
Lead Sponsor
arayana Medical College and Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Weight 40-70 kg, BMI <35kg/m2.

2)Patient aged between 20- 40years.

3)ASA II listed for elective Caesarean section

Exclusion Criteria

1) Patients without valid informed and written risk consent

2) ASA III and IV

3) Patients with BMI >35kg/m2.

4) Use of oral anticoagulants

5) Allergy to study drugs

•Local infection

•Severe psychiatric disorders

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the effect of 4mg dexamethasone and 8mg dexamethasone added to levobupivacaine on postoperative blood sugarsTimepoint: 2hours postoperatively and fasting blood sugars on postoperative day 1,2 and 3
Secondary Outcome Measures
NameTimeMethod
To assess the occurrence of surgical site infection in both the groupsTimepoint: 30 days;To assess VAS Scores in both the groupsTimepoint: immediately,6hr,12hr,24 hrs
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