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The effect of ginger versus metoclopramid in prevention of nausea and vomiting in patients undergoing cesarean section with spinal anaesthesia

The effect of ginger versus metoclopramid in prevention of nausea and vomiting in patients undergoing cesarean section with spinal anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201611028611N3
Enrollment
180
Registered
2017-01-31
Start date
2016-10-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pregnancy. normal pregnancy

Interventions

Intervention 1: Intervention/Control 1: First group received 1 gr ginger capsule (product of Dineh pharmaceutical company.Qazvin)30 minutes before induction of anaesthesia. Intervention 2: Interven
Treatment - Drugs
Intervention/Control 1: First group received 1 gr ginger capsule (product of Dineh pharmaceutical company.Qazvin)30 minutes before induction of anaesthesia
Intervention/Control 2 : Second group received 10 mg ampule of metoclopramid (product of Caspian pharmaceutical company.Gilan)30 minutes before induction of anaesthesia.

Sponsors

Vice-Chancellor for Research of Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18-40 years old patients undergoing cesarean with spinal anaesthesia. Exclusion criteria: Any history of an allergy to metoclopramid and ginger; any history of gastrointestinal surgery on stomach, upper GI and gall bladder; any history of bleeding disorder (haemophilia, ITP); any contraindication to intrathecal or epidural anaesthesia (Arnold- chiari); high risk patient for anaesthesia (ASA III, IV); any history of using antiemetic drugs and metoclopramid doses at 24 hours befor the surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Times of nausea. Timepoint: Evaluate and record during the operation and 1, 2, 6 and 24 hours after surgery. Method of measurement: Self-report tool.;Severity of Vomiting. Timepoint: Evaluate and record during the operation and 1, 2, 6 and 24 hours after surgery. Method of measurement: Self-report tool.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Hamideh Pakniat

Kowsar Hospital

pakniat110@yahoo.com+98 28 3333 6001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 18, 2026