Phenylephrine

2

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

Condition / disease
Location
Status: Recruiting

Comparison of Two Different Doses of Phenylephrine on Oxytocin Hemodynamic Effect

Cesarean section is one of the commonly performed surgical procedures in the world. Once baby is delivered during the surgical procedure anesthesiologist administer Oxytocin drug through IV cannula which helps the Uterus to contract so that excessive blood loss doesnt occur. But this is associated with fall in blood pressure frequently requiring administration of medications to treat low blood pressure. The most frequently used drug is phenylephrine which can administered along with oxytocin to prevent fall in blood pressure. This study will compare to different doses of Phenylephrine to prevent fall in blood pressure.

Participants needed: 112
Trial details
Phase: Phase 4Age: 20-40Biological sex: FemaleType: InterventionalSponsor: Rawalpindi Medical CollegeUpdated: Feb 24, 2026Locations: 1
Eligibility criteria

Patients having a placental abnormality [+2]

Status: Recruiting

Clinical Determinants and Adverse Reactions to Tropicamide/Phenylephrine in Hospitalized Patients.

To evaluate the association between clinical determinants and the occurrence of adverse drug reactions in hospitalized patients who received tropicamide/phenylephrine 8 mg/50 mg/mL. An ambispective, interventional, longitudinal study will be conducted to actively identify adverse reactions to tropicamide/phenylephrine 8 mg/50 mg/mL, as well as the clinical determinants that may predispose patients to the occurrence of an adverse drug reaction (ADR). Data will be collected through the administration of a questionnaire and measurement of vital signs prior to the administration of tropicamide/phenylephrine 8 mg/50 mg/mL, and subsequently at 5 minutes, 15 minutes, 30 minutes, 1 hour, 2 hours after administration, with the aim of establishing an association between these variables.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Instituto de Oftalmología Fundación Conde de ValencianaUpdated: Sep 17, 2025Locations: 1
Eligibility criteria

Patients who have authorized participation in the study by signing informed cons... [+5]

Allergy to any component of the formulation.