Skip to main content
Clinical Trials/CTRI/2021/06/034068
CTRI/2021/06/034068CompletedNot Applicable

POSTOPERATIVE ANALGESIC EFFECT OF INTRAPERITONEAL ROPIVACAINE WITH AND WITHOUT MAGNESIUM SULFATE IN LAPAROSCOPIC CHOLECYSTECTOMY-A PROSPECTIVE OBSERVATIONAL STUDY

DNB Resident Dissertation No financial support1 site in 1 country44 target enrollmentStarted: June 30, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
44
Locations
1
Primary Endpoint
To assess the

Study Overview

Brief Summary

the study is to compare the duration of analgesia and incidence of pain after intraperitoneal instillation of ropivacaine with and without magnesium sulphate in patints undergoing elective laparoscopic cholecystectomy,secondarily the study aims to note the post drug instillation hemodynamics,incidence and severity of postoperative nausea and vomiting

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

Eligibility Criteria

Ages
25.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •PATIENTS WHO ARE ASA CLASS 1 OR 2 UNDERGOING ELECTIVE LAPROSCOPIC SURGERY BMI -18 TO 30.

Exclusion Criteria

  • •PATIENT WITH ECG SHOWING CONDUCTION ABNORMALITIES PREGNANT AND BREASTFEEDING PATIENT ON BETA BLOCKERS PATIENT WITH CHRONIC PAIN ON OPIOIDS AND OTHER ANALGESICS HISTORY OF ALLERGY TO STUDY DRUGS SURGERY DURATIONS MORE THAN THREE HOURS CONVERSION TO OPEN PROCEDURE EMERGENCY CHOLYCYSTECTOMY PATIENTS REQUIRING COMMON BILE DUCT EXPLORATION.

Outcomes

Primary Outcomes

To assess the

Time Frame: baseline,1 hour,2hour.6 hour,12 hour,24 hour

1.duration of analgesia after intraperitoneal instillation of ropivacaine with and without magnesium sulphate,

Time Frame: baseline,1 hour,2hour.6 hour,12 hour,24 hour

3.total doses of rescue analgesics in each groups

Time Frame: baseline,1 hour,2hour.6 hour,12 hour,24 hour

4.type of pain.

Time Frame: baseline,1 hour,2hour.6 hour,12 hour,24 hour

2.Mean pain scores during 24 hour ,

Time Frame: baseline,1 hour,2hour.6 hour,12 hour,24 hour

Secondary Outcomes

  • Secondary objective(To study the post instillation hemodynamic changes in terms of heart rate(HR), systolic blood pressure(SBP), diastolic blood pressure(DBP), Oxygen saturation (SpO2), End Tidal Co2 (EtCO2) and postoperative nausea and vomiting(PONV))

Investigators

Sponsor
DNB Resident Dissertation No financial support
Sponsor Class
Other [DNB Resident Thesis Protocol]

Study Sites (1)

Loading locations...

Similar Trials