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Pregnancy clinical trials

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NCT ID: NCT00966771 Completed - Pregnancy Clinical Trials

The Copper T380A IUD vs. Oral Levonorgestrel for Emergency Contraception

IUD EC
Start date: October 2009
Phase: N/A
Study type: Observational

The purpose of this study is to see if women presenting for emergency contraception (EC) and choose the copper intrauterine device (IUD) will have fewer unplanned pregnancies in the next year compared to women who choose oral levonorgestrel for EC. The study will also compare use of an effective method of contraception in the year after they received EC.

NCT ID: NCT00966537 Recruiting - Pregnancy Clinical Trials

The 3-Dimensional Ultrasound for Fetal Anomaly Scan

Start date: May 2008
Phase: N/A
Study type: Observational

The aim of this study is 1) to study the clinical application of 3D/4D ultrasound for fetal scanning during pregnancy; 2) ) to study the clinical application of 3D/4D ultrasound for pelvic scanning; 3) to demonstrate how to optimally display the different organs. 4) to correlate our findings with other diagnostic tools like MRI, CT; 5) to correlate our findings with clinical outcome.

NCT ID: NCT00961987 Not yet recruiting - Pregnancy Clinical Trials

Innovation to Providing Interprofessional Maternity Care

Start date: October 2009
Phase: N/A
Study type: Interventional

The aim of this pilot project is to determine if there are differences in patient outcomes and healthcare utilization between patients randomly assigned to usual care (a collaborative model of maternity care with co-located healthcare professionals but with referrals to off-site obstetricians) or to a collaborative model of maternity care with co-located healthcare professionals, including obstetricians. It is hypothesized that by creating a seamless interface between obstetrical consultation and ongoing longitudinal maternity care, patient outcomes (birth outcome data), patient satisfaction and healthcare utilization, including number of outpatient visits, ultrasounds, laboratory tests, consultations, etc, will be improved in the intervention group compared with the group receiving usual care. The results could potentially lead to other sites adopting this innovative model of maternity healthcare delivery.

NCT ID: NCT00957476 Completed - Obesity Clinical Trials

Omega-3 Supplementation Decreases Inflammation and Fetal Obesity in Pregnancy

Start date: September 2009
Phase: N/A
Study type: Interventional

Randomized, double-blind placebo controlled trial of fish oil to decrease inflammation in pregnancy.

NCT ID: NCT00954811 Recruiting - Pregnancy Clinical Trials

Luteal Supplementation With Rec-LH After GnRH-agonist Triggering in In Vitro (IVF)

Start date: September 2005
Phase: Phase 4
Study type: Interventional

Our aim is to access whether we can achieve equivalent pregnancy rates by the addition of six doses of luteal support with recLH after agonist triggering for IVF cycles in the absence of OHSS.

NCT ID: NCT00954265 Active, not recruiting - Pregnancy Clinical Trials

Pregnancy Rates in IVF After Ovulation Triggering With Recombinant or Urinary Human Chorionic Gonadotrophin (HCG)

Start date: August 2005
Phase: Phase 3
Study type: Interventional

To access whether the ovulation triggering with rec-HCG instead urinary-HCG has any impact on the blastulation rate and pregnancy rate of patients undergoing IVF treatment

NCT ID: NCT00950235 Completed - Obesity Clinical Trials

Weight Management for Improved Pregnancy Outcomes

Healthy Moms
Start date: October 2009
Phase: N/A
Study type: Interventional

This study will examine the safety and effectiveness of a dietary intervention in pregnant women. Women who are obese will be invited to participate. The control arm will receive routine prenatal care and one in-person nutritional and dietary counseling session to promote healthy eating during their pregnancy. The intervention arm will receive a more intensive dietary program that will include in-person counseling and group support sessions. The goal of the intervention will be weight maintenance (weight at 2 weeks after delivery should be within 3% of baseline weight) and avoidance of postpartum weight retention

NCT ID: NCT00942097 Completed - Pregnancy Clinical Trials

Homeopathic Medication and Nutritional Oriented Diet to Treat Overweight Pregnant Women With Mental Disorder

Start date: August 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of homeopathic treatment in pregnant women with overweight and class I obesity with suspicion of a mental disorder.

NCT ID: NCT00938600 Completed - Pregnancy Clinical Trials

Antenatal Vitamin D3 Dose-finding and Safety Study

AViDD-1
Start date: July 2009
Phase: Phase 1
Study type: Interventional

This is a preliminary study of oral vitamin D3 supplementation in pregnant and non-pregnant women of reproductive age in Bangladesh. The primary objective of the study is to identify a dose of vitamin D3 that can safely be administered during pregnancy to improve the vitamin D status of the mother and infant.

NCT ID: NCT00936195 Withdrawn - HIV Infections Clinical Trials

Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in Pregnant and Breastfeeding Women : a Phase 3 Trial

UMA
Start date: January 2010
Phase: Phase 3
Study type: Interventional

To assess the maternal and infant safety of a single daily fixed-dose combination of TDF/FTC/EFV (Atripla®), compared to the association of LPV/r (Kaletra® or Aluvia®) and 3TC/ZDV (Combivir®) given to African women to prevent overall MTCT in populations practicing breastfeeding.