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Pregnancy clinical trials

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NCT ID: NCT00702338 Completed - Pregnancy Clinical Trials

Pregnancy and Neonatal Follow-up of Ongoing Pregnancies Established in Clinical Trial P05693 (P05713)

Care
Start date: May 15, 2008
Phase:
Study type: Observational

The objective of follow-up study P05713 is to evaluate whether corifollitropin alfa (Org 36286) treatment for the induction of monofollicular growth in women who underwent ovulation induction (OI) in base study P05693 (NCT00697255) is safe for pregnant participants and their offspring.

NCT ID: NCT00702234 Completed - Pregnancy Clinical Trials

Pregnancy and Neonatal Follow-up of Ongoing Pregnancies Established in Clinical Trial P05714 (Care Program)(P05715)

Care
Start date: February 15, 2007
Phase:
Study type: Observational

The objective of this trial is to evaluate whether corifollitropin alfa (Org 36286) treatment for the induction of multifollicular growth in women undergoing controlled ovarian stimulation (COS) prior to in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) is safe for pregnant participants and their offspring. In addition, a primary efficacy variable, live birth rate, was evaluated.

NCT ID: NCT00702195 Completed - Pregnancy Clinical Trials

Pregnancy and Neonatal Follow-up of Ongoing Pregnancies Established During Phase II Clinical Trials of Org 36286 (Study 38817)(P06054)(COMPLETED)

Start date: January 1, 2002
Phase:
Study type: Observational

The objective of this trial was to evaluate whether Org 36286 treatment in any Phase IIa clinical development trial of Org 36286 for OI or COH in assisted reproductive treatment programs was safe for pregnant subjects and their offspring. Data from subjects who participated in Trials 38805 and 38807 and became pregnant were evaluated.

NCT ID: NCT00699595 Completed - Pregnancy Clinical Trials

Hormonal Effects on Pain Perception

HEPP
Start date: September 2008
Phase: N/A
Study type: Observational

To investigate if labor pain is affected by mother's hormone levels. The hormonal effects of pregnancy are well documented. Although differences in pain sensitivity between women and men are partly attributable to social conditioning and to psychosocial factors, many laboratory studies of humans have described sex differences in sensitivity to noxious stimuli, suggesting that biological mechanisms underlie such differences. Some animal studies have suggested that sensitivity to pain decreases during pregnancy because of the progressive activation of endogenous pain inhibitory systems. This effect may be mediated by pregnancy-associated hormones, in particular progesterone.

NCT ID: NCT00686062 Completed - Pregnancy Clinical Trials

Evaluation of a Decision Assisting Tool for Prenatal Testing

Start date: April 2001
Phase: N/A
Study type: Interventional

This is a randomized study of an interactive, computerized descision-assisting tool for prenatal testing decision making (PT Tool) versus standard educational booklets distributed to all pregnant women by the State of California (control). We hypothesize that, compared to controls, women randomized to view PT Tool will have greater knowledge about prenatal testing and its potential outcomes and better risk comprehension, and that they will be more satisfied with the intervention and have lower decisional conflict.

NCT ID: NCT00685932 Completed - Pregnancy Clinical Trials

Mobius® Post-cesarean Pain Randomized Control Trial

Start date: July 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether the use of the Mobius® retractor decreased post-operative pain after cesarean section verses conventional retractor use. Based on clinical experience and a pilot study, we suspect that the retractor will decrease overall pain as well as lateral pain.

NCT ID: NCT00685672 Completed - Pain Clinical Trials

Safety of Epidural Fentanyl and Adrenalin During Childbirth

Start date: August 2008
Phase: Phase 4
Study type: Interventional

Investigation of pharmacokinetic effects of combining fentanyl and adrenalin in the epidural solution given to women in childbirth

NCT ID: NCT00683202 Completed - Pregnancy Clinical Trials

Low-Dose Aspirin in in Vitro Fertilization (IVF) and Intracytoplasmic Sperm Injection (ICSI) Treatments

Start date: March 2001
Phase: N/A
Study type: Interventional

In this study we hypothesized that low-dose aspirin therapy (100 mg daily) improves ovarian responsiveness, uterine haemodynamics and clinical pregnancy rates in unselected subjects undergoing IVF/ICSI when the treatment is started concomitantly with controlled ovarian hyperstimulation.

NCT ID: NCT00682201 Completed - Pregnancy Clinical Trials

Hemodynamic Changes During Normal Pregnancy

Start date: August 2007
Phase: N/A
Study type: Observational

Prospective, observational study of the changes in hemodynamic variables such as blood pressure, cardiac output, systemic vascular resistance, and of changes in respiratory variables such as vital capacity, and functional residual volume.A cohort study of 100 healthy pregnant women tested with non-invasive methods during pregnancy and 6 months after delivery.

NCT ID: NCT00669396 Completed - Pregnancy Clinical Trials

Copper T380 IUD Versus Oral Levonorgestrel for Emergency Contraception vs. Plan B for Emergency Contraception

Start date: April 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to see if women presenting for emergency contraception (EC) are willing to accept the copper intrauterine device (IUD). This study will also compare the use of effective methods of contraception between women who selected the copper IUD or Plan B 6 months after they received EC.