Granisteron Versus Metoclopramide in Laparoscopic Cholecystectomy

NCT ID: NCT04899817

Last Updated: 2021-05-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-31

Study Completion Date

2022-04-30

Brief Summary

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Study aims at comparing the effect of granisteron with that of metoclopramide in patients undergoing lab cholecystectomy

Detailed Description

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Post operative nausea and vomitting is Avery common complication of laparoscopic surgery in that study we will compare between granisteron and metoclopramide as aprophlaxis against post operative nausea and vomitting

Conditions

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Nausea and Vomiting, Postoperative

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Group G

will receive granisteron 1mg after induction of general anesthesia

Group Type ACTIVE_COMPARATOR

Granisetron

Intervention Type DRUG

The drug is given after induction of general anesthesia

Group C

Will receive metoclopramide 10 mg after induction of general anesthesia

Group Type PLACEBO_COMPARATOR

Granisetron

Intervention Type DRUG

The drug is given after induction of general anesthesia

Interventions

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Granisetron

The drug is given after induction of general anesthesia

Intervention Type DRUG

Other Intervention Names

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Granitryl

Eligibility Criteria

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Inclusion Criteria

* both sexes Age between 18 and 60 years ASA1 2 3 Lap cholecystectomy under general anesthesia

Exclusion Criteria

* patients refusal Pregnancy and breastfeeding Hepatic or renal disease ASA4 5 Allergy to the drug
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Lyali Salah Dardeer

Assistant lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Eman M Esmail

Role: STUDY_DIRECTOR

Assiut University

Locations

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Assiut university hospital

Asyut, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Layali Dardeer

Role: CONTACT

01096928662

Facility Contacts

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Layali S Dardeer

Role: primary

01096928662

Other Identifiers

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Antiemetics in lab cholecystec

Identifier Type: -

Identifier Source: org_study_id

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