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384 studies found for:    Open Studies | "Obstetric Labor Complications"
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Rank Status Study
21 Not yet recruiting Impact of Analgesia on Success of External Version: Comparison of Spinal Anesthesia Versus Sedation
Condition: Breech Presentation
Interventions: Drug: Midazolam;   Drug: Bupivacaine
22 Recruiting Pharmacokinetics (PK) and Modeling of Betamethasone Therapy in Threatened Preterm Birth
Condition: Premature Labor
Intervention:
23 Recruiting A Comparative Study of the Effect of Two Partographs on the Cesarean Section Rate in Women in Spontaneous Labour
Condition: Dystocia
Interventions: Other: New partograph based on the studies of Neal and Lowe;   Other: Classical partograph
24 Not yet recruiting Tocolytic Therapy for Preterm Labor in Multiple Gestation
Condition: Labor Preterm Multiple
Interventions: Drug: Atosiban;   Drug: Nifedipine
25 Recruiting Family Nurture Intervention in the NICU
Conditions: Premature Birth;   Obstetric Labor, Premature
Interventions: Behavioral: Family Nurture Intervention;   Behavioral: Standard Care
26 Recruiting Evaluation of the Role of Vaginal Progesterone in Prevention of Preterm Labor in Twin Gestation With Short Cervix: Randomised Controlled Trial
Conditions: Twins, Dizygotic [M01.438.873.920];   Obstetric Labor, Premature [C13.703.420.491]
Interventions: Drug: Progesterone;   Other: Placebo
27 Recruiting EOS® Versus Spiral CT Technique for Achieving a Pelvimetry in Suites of Obstructed Labor.
Condition: Pregnancy
Interventions: Device: EOS;   Device: Spiral CT pelvimetry
28 Recruiting Vaginal Progesterone Versus Cervical Cerclage for Pregnant Women With Short Cervix and History of PTL and/or MTM
Condition: Premature Labour
Interventions: Drug: Progesterone;   Procedure: Cervical cerclage
29 Not yet recruiting Prevention and Treatment of Premature Labour for Asymptomatic Pregnant Women
Condition: Premature Labour
Intervention: Device: ultrasound
30 Recruiting Efficacy and Safety of MgSO4 as Tocolytics Compared to Ritodrine in Preterm Labor
Condition: Preterm Labor
Interventions: Drug: MgSO4;   Drug: YTP(Ritodrine)
31 Recruiting Comparison Between Natural Progesterone and Vaginal Pessary for the Prevention of Spontaneous Preterm Birth
Conditions: Preterm Labor;   Premature Birth
Interventions: Drug: natural progesterone;   Device: cervical pessary
32 Recruiting Intrapartum Rapid GBS Testing in Patients Presenting With Threatened Preterm Labor
Condition: Group B Streptococcus
Intervention: Other: GBS culture and real time PCR
33 Recruiting Impact of Complementary Medicine Techniques (Therapeutic Touch and Hypno Analgesia) on the Term of Delivery of Patients Hospitalized for Preterm Labor (Hypnorelax)
Condition: Premature Birth
Interventions: Other: Touching relaxant;   Other: Hypnoses
34 Recruiting Comparison of Low-dose and High-dose Oxytocin Regimens for Labor Augmentation
Condition: Dystocia
Interventions: Drug: Oxytocin;   Other: Sodium Chloride 0.9%
35 Recruiting Prevention of Preterm Birth in Singletons Using Pessary After Resolutive Threatened Preterm Labor
Condition: Preterm Birth
Intervention: Device: Silicone pessary
36 Recruiting Indomethacin PK and PD Therapy in Pregnancy
Conditions: Premature Labor;   Pregnancy;   Premature Birth
Intervention:
37 Recruiting Nifedipine or Nifedipine Plus Indomethacin for Treatment of Acute Preterm Labor
Condition: Preterm Labor
Interventions: Drug: Nifedipine;   Drug: Indomethacin
38 Not yet recruiting Vaginal Progesterone for the Prolongation of Pregnancy After Arrested Pre-term Labor
Condition: Preterm Labor
Interventions: Drug: micronized progesterone 400 mg (Utrogestan);   Other: Placebo
39 Recruiting A Phase III Efficacy and Safety Study of Intravenous Retosiban Versus Placebo for Women in Spontaneous Preterm Labor
Condition: Obstetric Labour, Premature
Interventions: Drug: Retosiban IV infusion;   Drug: Placebo IV infusion
40 Recruiting Management of Acute Preterm Labor: Nifedipen Alone or Combined With Cildenafil Citrate
Condition: Labor Preterm Requiring Hospitalization
Interventions: Drug: nifedipen;   Drug: Sildenafil

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Study has passed its completion date and status has not been verified in more than two years.