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The Effect of Intravenous Granisetron and Ondansetron in Patients Undergoing Cesarean Section

NCT04613726 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2020-11-03

No results posted yet for this study

Summary

This study compared the effects of prophylactic intravenous (IV) infusion of ondansetron and granisetron before the spinal anesthesia on hemodynamic parameters in patients undergoing elective cesarean section.

Conditions

  • Vomiting, Postoperative
  • Postoperative Complications
  • Hypotension

Interventions

DRUG

ondansetron

group consisted of receiving IV 8 mg ondansetron diluted in 10 ml of normal saline

DRUG

Granisetron

Another comparator group consisted of receivingIV 3 mg granisetron diluted in 10 ml of normal saline

DRUG

Saline

Control group consisted of patients receiving IV 10 ml normal saline

Sponsors & Collaborators

  • Ataturk University

    lead OTHER

Principal Investigators

  • Mehmet AKSOY, Assoc.Prof. · Faculty of Medicine, Ataturk University, Erzurum, Turkey

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-12-03
Primary Completion
2019-12-12
Completion
2020-01-01

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04613726 on ClinicalTrials.gov