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Peripheral Nerve Stimulator guided Erector Spinae Plane Block for Postâ??operative pain relief following Abdominal Hysterectomies

Not Applicable
Completed
Conditions
Health Condition 1: N859- Noninflammatory disorder of uterus, unspecified
Registration Number
CTRI/2019/08/020851
Lead Sponsor
TEERTHANKAR MAHAVEER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

American Society of Anaesthesiologists (ASA) grade I & II patients

Patients with BMI 18.5-22.9 kg/m2

Exclusion Criteria

Patients refusal

Hypersensitivity to local anesthetics

Chronic analgesic therapy

Any surgery extending more than 120 minutes

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patient reported pain intensity using Visual Analogue Scale (VAS) & time for first analgesic requirementTimepoint: Prior to administration of Erector Spinae plane Block immediately after surgery 1hr 2hrs 4hrs 6hrs 12hrs 18hrs <br/ ><br>and 24 hrs in post operative period
Secondary Outcome Measures
NameTimeMethod
Haemodynamic changes (MAP SBP DBP HR) <br/ ><br>Complications (if any)Timepoint: Prior to administration of Erector Spinae plane Block immediately after surgery 1hr 2hrs 4hr 6hrs 12hrs 18hrs <br/ ><br>and 24 hrs in post operative period
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