Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 5:20 PM
Ignite Modification Date:
2025-12-26 @ 5:20 PM
NCT ID:
NCT06513806
Eligibility Criteria:
Inclusion Criteria:
* elective for caesarian section presence of post-spinal shivering, defined as involuntary muscle contractions occurring within operative and early recovery period after cesarean delivery.
* Age 18 - 45
Exclusion Criteria
* Inability to provide informed consent.
* Previous allergies or sensitivities to granisetron or pethidine.
* Current use of medications that may interact with granisetron or pethidine.
* Presence of other conditions that may contraindicate the use of granisetron or pethidine, such as known liver or kidney disease.
* Patients who are too short (\<140 cm) or too tall (\>190 cm)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT06513806
Study Brief:
Protocol Section:
NCT06513806