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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04721054
Other study ID # 104589
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2018
Est. completion date October 31, 2019

Study information

Verified date January 2021
Source Armed Forces Hospital, Pakistan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Eighty two patients planned to undergo elective laparoscopic cholecystectomy were divided into two groups, T and G, randomly. In Group T all patients underwent laparoscopic cholecystectomy under thoracic epidural anesthesia with 12mlof 0.25% bupivacaine and 1% lignocaine plain whereas in group G all patients underwent surgery under general anesthesia. Intra-operative heart rate, mean arterial pressure (MAP) and post operative opioid consumption in first 24hrs were recorded as primary outcomes whereas presence or absence of respiratory complication and duration of hospital stay as secondary outcome.


Recruitment information / eligibility

Status Completed
Enrollment 82
Est. completion date October 31, 2019
Est. primary completion date October 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: 1. patients having ASA statusI-III 2. age more than 18 years, 3. both genders 4. planned to undergo laparoscopic cholecystectomy Exclusion Criteria: 1. Patients who did not give consent, 2. Allergic to local anesthetic 3. Hemodynamically unstable, 4. Pregnant, full stomach patients

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Thoracic epidural effect on heart rate in Laparoscopic Cholecystectomy (bupivacaine and lignocaine)
patients in epidural anesthesia were given epidural anesthesia and assessed for heart rate and mean arterial pressure
general anesthesia effect on heart rate in Laparoscopic Cholecystectomy
patients in general anesthesia were given epidural anesthesia and assessed for heart rate and mean arterial pressure

Locations

Country Name City State
Pakistan Military Hospital Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Armed Forces Hospital, Pakistan

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary effectiveness of thoracic epidural anesthesia with general anesthesia for Laparoscopic cholecystectomy in terms of change in heart rate during surgery in immediate 24 hours-heart rate. the efficacy of thoracic epidural anesthesia was compared with general anesthesia for laproscopic cholecystectomy in the immediate post operative period in terms of intra operative heart rate. changes in heart rate at 24 hours of surgery.
Primary effectiveness of thoracic epidural anesthesia with general anesthesia for Laparoscopic cholecystectomy in terms of change in mean arterial blood pressure during surgery in immediate 24 hours-mean arterial blood pressure. efficacy of thoracic epidural anesthesia was compared with general anesthesia for laproscopic cholecystectomy in the immediate post operative period in terms of mean arterial blood pressure intra operatively and in immediate post operative period changes in mean arterial pressure at 24 hours of surgery
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