Skip to content

Comparison Between Drugs for Control of Emetic Attacks During Caesarean Delivery

Comparison Between Propofol, Ondansetron and Pregabalin for Control of Emetic Attacks During Caesarean Delivery With Spinal Anesthesia: Randomized Clinical Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06300346
Enrollment
90
Registered
2024-03-08
Start date
2024-03-01
Completion date
2024-08-18
Last updated
2024-03-08

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

Conditions

Emetic Attacks During Caesarean Delivery With Spinal Anesthesia

Brief summary

Single shot spinal anesthesia is widely used for most surgical operations especially in obstetric such as hysterectomy, tubal ligation after vaginal delivery, cesarean and curettage etc.; however, in general, cesarean is considered as the most common indication for spinal anesthesia in pregnant women Intra-operative nausea and vomiting/retching (NVR) may be experienced by 20% to 80% of women undergoing cesarean section (CS) with subarachnoid anesthesia (SA) in the absence of antiemetic prophylaxis. Different treatment options are available to reduce post operative nausea and vomiting (PONV) so we will make a Comparison between Propofol, Ondansetron and Pregabalin for Control of Emetic Attacks during Caesarean Delivery with Spinal Anesthesia

Interventions

DRUGPropofol

Ondansetron

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Age: 21-40 years old. * Physical status American Society of Anesthesiologists (ASA)I&II. * Body mass index (BMI) \< 35&\>20 kg/m2. * Elective uncomplicated cesarean section under spinal anesthesia.

Exclusion criteria

* Patient refusal. * Patients with known history of allergy to study drugs. * Advanced hepatic, renal and respiratory diseases. * Psychological and mental disorders. * Patient with reduced level of consciousness. * Hypertensive, cardiac, and diabetic patients. * Patients receiving anticoagulants therapy or suspected coagulopathy.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of nausea and vomiting with spinal anesthesia5 monthsTo compare between Propofol, Ondansetron and Pregabalin for control of emetic attacks during caesarean delivery with spinal anesthesia.

Secondary

MeasureTime frameDescription
Measurement of hemodynamics postoperative5 monthsMeasurement of hemodynamics postoperative and Incidence of other side effects as :hypotension measured by non invasive blood pressure monitoring

Contacts

Primary ContactEbtihal A Abd-Ellateef, resident
ebtehalahmed@med.sohag.edu.eg01119925603
Backup ContactAhmed M Abd-Elmaboud, assistant professor
01150217744

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026