Hyoscine ButylBromide for Intrapartum Analgesia

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Status Not yet recruiting

Clinical Trial Summary

The aim of this study is to assess whether hyoscine butylbromide is as effective as pethidine for analgesia during the first stage of labor.

n/a

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

NCT number	NCT02557087
Study type	Interventional
Source	Ain Shams Maternity Hospital
Contact
Status	Not yet recruiting
Phase	Phase 2
Start date	September 2015
Completion date	March 2016

See also
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Active, not recruiting	`NCT03167905` - CODEPAD (Collaborative Outcomes of DEpression and Pain Associated With Delivery)	Phase 2/Phase 3
Completed	`NCT02009722` - Intrathecal Opioids for Pain Control After Cesarean Delivery: Determining the Optimal Dose	Phase 4
Active, not recruiting	`NCT03805607` - IV Ketorolac on Platelet Function Post-Cesarean Delivery	Phase 4
Completed	`NCT03574441` - Intrapartum Epidural Catheter Displacement: Dressing Methods	N/A
Completed	`NCT02920489` - Individualized Timing of Analgesia and Effectiveness of Labor Analgesia	N/A
Completed	`NCT02823418` - Neuraxial Labor Analgesia and the Incidence of Postpartum Depression
Not yet recruiting	`NCT05977361` - Intrathecal Catheter Placement Versus Resiting Epidural Catheter After Dural Puncture in Obstetric Patients	N/A