Trials / Terminated
TerminatedNCT00525486
Extended Release Nifedipine Treatment as Maintenance Tocolysis to Prevent Preterm Delivery
Extended Release Nifedipine Treatment as Maintenance Tocolysis to Prevent Preterm Delivery:A Prospective Interventional Study
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- —
- Sponsor
- The Baruch Padeh Medical Center, Poriya · Other Government
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
To evaluate the treatment efficacy and safety usig extended release nifedipine, as maintenance therapy to pregnant women who were hospitalized and treated for preterm labor until 34 weeks' gestation. After the PTL will stop, we will randomize these women for the treatment group and the control (no treatment) group. The main outcome will be preterm delivery before 34 weeks' gestation. the secondary outcome will be the side effects of the medication and the newborn/mother health variables.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nifedipine extended release | Nifedipine extended release PO 30 mg X2/d until 34 weeks' gestation |
Timeline
- Start date
- 2007-12-01
- First posted
- 2007-09-05
- Last updated
- 2010-12-23
Source: ClinicalTrials.gov record NCT00525486. Inclusion in this directory is not an endorsement.