Pruritus Caused by Drug

2

Review clinical trials related to Pruritus Caused by Drug. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Comparison of Pruritus Incidence After Intrathecal Morphine 0.1 vs 0.2 mg in Cesarean Section

This study compares the incidence of pruritus (itching) requiring treatment between two doses of intrathecal morphine (0.1 mg vs 0.2 mg) when used for spinal anesthesia during cesarean section. The study aims to determine if the lower dose (0.1 mg) can reduce pruritus incidence while maintaining adequate pain relief.

Participants needed: 69
Trial details
Phase: Phase 4Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Khon Kaen UniversityUpdated: Jul 8, 2025Locations: 2
Eligibility criteria

Full-term pregnancy [+3]

Contraindication to spinal anesthesia or study drugs [+4]

Status: Recruiting

Ondansetron Use for Preventing Pruritus in Patients Undergoing Cesarean Section

Opioids are often added with a local anesthetic to enhance the duration and quality of spinal anesthesia for cesarean delivery patients. However, spinal opioids are associated with a wide variety of side effects such as nausea, vomiting, (N/V) and pruritus (itching). The occurrence of pruritus can vary between 30% and 100% making pruritus the most common side-effect of intrathecal opioids and this rate is even higher in pregnant patients. Pruritus may require treatment which can be ineffective or sometimes reverse the analgesic effect of the opioids. Ondansetron is a safe and very commonly used Serotonin receptor antagonist treatment for local anesthetic opioid-induced pruritus used in pregnancy. The effect of different administration times of ondansetron in reducing pruritus or N/V in cesarean section (CS) cases has not been extensively studied and thus, this prospective study can help guide future clinical management of side effects caused by spinal intrathecal morphine administration.

Participants needed: 66
Trial details
Phase: Phase 1Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Wayne State UniversityUpdated: Mar 28, 2025Locations: 1
Eligibility criteria

American Society of Anesthesiologists (ASA) physical status 1-3 [+2]

Patients with an ASA physiological assessment greater than grade 3 [+20]