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Pregnancy clinical trials

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NCT ID: NCT00315029 Completed - Pregnancy Clinical Trials

Patient-Centered Implementation Trial for Single Embryo Transfer

Start date: November 2006
Phase: N/A
Study type: Interventional

Background: The number of multiple pregnancies is considered to be the most important adverse effect of in vitro fertilisation (IVF) and intracytoplasmic sperm injection (ICSI). IVF or ICSI with transferring only one embryo, elective single embryo transfer (eSET), will reduce this incidence remarkably. Unfortunately, former research has documented that cycles with SET maintain lower pregnancy rates compared to double embryo transfer (DET). Implementation of eSET will require a carefully chosen and thoroughly defined implementation strategy focussed on the couple undergoing the subfertility treatment. This trial will investigate the (cost)effectiveness of a combined patient centred implementation strategy. Objective: The main aim is to compare the effectiveness and costs of implementation of elective single embryo transfer (eSET) in in vitro fertilisation (IVF) and intracytoplasmic sperm injection (ICSI), between usual care and a combined patient-centred strategy. Study design: A randomised controlled trial Study population: Couples with a female age less than 40 years ongoing an IVF/ICSI treatment in 2 of the 13 Dutch IVF centres and their 4 satellite/transport centres. Intervention A combined patient centred implementation strategy for eSET in IVF/ICSI. The strategy consists of counselling through an evidence based decision aid and reimbursement of a 4th cycle if couples have chosen for eSET in the first 2 cycles. Primary study parameters/outcome of the study: the eSET occurrence rate, pregnancy outcomes and cost-effectiveness of the combined strategy. Secondary study parameters/outcome of the study: - patient knowledge - patient decisional conflict - patient satisfaction - IVF/ICSI treatment outcome.

NCT ID: NCT00312585 Completed - Pregnancy Clinical Trials

Acupuncture for the Prevention of Postdates Pregnancy

Start date: February 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess if acupuncture can shorten the time to delivery for women who are experiencing their first, full-term pregnancy.

NCT ID: NCT00294242 Not yet recruiting - Pregnancy Clinical Trials

Safety Study of Membrane Sweeping in Pregnancy

Start date: February 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if routine membrane sweeping in uncomplicated term pregnancies increases the rate of pre-labor rupture of membranes.

NCT ID: NCT00293644 Completed - Pregnancy Clinical Trials

Pre-emptive Treatment of Severe Nausea and Vomiting of Pregnancy

Start date: February 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether pre-emptive use of a delayed release combination of pyridoxine hydrochloride and doxylamine succinate (Diclectin®), before eruption of symptoms of Nausea and vomiting of pregnancy and hyperemesis gravidarum, will reduce the incidence of severe forms of this syndrome/HG.

NCT ID: NCT00291044 Completed - Pregnancy Clinical Trials

HSV Seroprevalence and Diagnosis of Genital Herpes in Pregnant Women

Start date: September 2005
Phase: N/A
Study type: Observational

Brief summary: The current management guidelines recommended by ACOG rely on history as a screening method to determine pregnant women who are at risk for transmitting herpes to their newborn. History fails completely in identifying the women most at risk of transmitting herpes to their newborn - the seronegative woman who acquires a primary infection from her partner during pregnancy. Despite recent advances, both pregnant women and newborns continue to be at risk of acquiring herpes infection. Genital herpes infections are epidemic in the United States. In the early 1990's, 25% of women in the US were seropositive for the HSV-2 antibody. These numbers are likely higher now. The incidence of neonatal herpes in the US cannot be accurately estimated since it is not a reportable disease. However, in some areas of the US, the incidence is 1 in 3,200 live births which would translate to an incidence of approximately three infants a day in the US . In other areas of the US, the incidence is even higher, approaching 1 in 1,500 liveborns. This protocol examines patient acceptance of HSV-1 and HSV-2 type specific serologic testing and assesses patient counseling tools. In addition, seroprevalence of HSV-2 in pregnant patients will be collected and evaluated.

NCT ID: NCT00290173 Completed - Pregnancy Clinical Trials

Ritodrine in Oral Maintenance of Tocolysis After Active Preterm Labor

Start date: n/a
Phase: N/A
Study type: Interventional

This is a trial comparing the efficacy of oral ritodrine in the form of sustained release capsules for the maintenance of uterine quiescence after successfully treated episode of threatened preterm labor.

NCT ID: NCT00282204 Completed - Pregnancy Clinical Trials

Hypnosis Antenatal Training for Childbirth (HATCh): a Randomised Controlled Trial

Start date: December 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Antenatal hypnosis is associated with a reduced need for pharmacological interventions during childbirth. This trial seeks to determine the efficacy or otherwise of antenatal group hypnosis preparation for childbirth in late pregnancy.

NCT ID: NCT00274261 Completed - Pregnancy Clinical Trials

Study of the Safety and Contraceptive Efficacy of C31G Compared to Conceptrol®

Start date: June 2004
Phase: Phase 3
Study type: Interventional

This is a multicenter, randomized, double-masked, controlled, phase III study of repeated use of C31G vaginal gel compared to Conceptrol® Vaginal Gel as the primary method of contraception over six months (183 days) and at least six cycles of use. In addition, there is an opportunity for subjects to continue with study treatment for up to twelve months (365 days) and twelve cycles of treatment upon completion of the first six months of treatment.

NCT ID: NCT00273637 Recruiting - Heart Failure Clinical Trials

Registry and Survey of Women With Pregnancy Related Cardiomyopathy

Start date: October 2005
Phase: N/A
Study type: Observational

The goal of this study is to better characterize peripartum cardiomyoapthy or pregnancy-related cardiomyopathy by enrolling as many PPCM survivors as possible using both direct and web-based methods of recritment. Patients will anser a questionnaire regarding the onset, progression, treatment and follow-up of their diagnosis as well as the psychosocial aspects of PPCM.

NCT ID: NCT00271219 Completed - Pregnancy Clinical Trials

RCT Comparing Methadone and Buprenorphine in Pregnant Women

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

Children born to women who abuse drugs have a high risk of being born with birth defects and developmental problems. Methadone is a drug that is commonly used for treating opioid dependence. However, its use by a pregnant woman can cause severe withdrawal symptoms in a newborn because of the prenatal exposure. The purpose of this study is to evaluate the effectiveness of buprenorphine, another drug, versus methadone in reducing withdrawal symptoms in children born to opioid-dependent women.