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Pregnancy clinical trials

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NCT ID: NCT01882738 Not yet recruiting - PREGNANCY Clinical Trials

Effect of Maternal BMI on Measurement of Cervical Length

Start date: July 2013
Phase: N/A
Study type: Observational

All consecutive pregnant patients in 2nd or 3rd trimester will be asked to participate. Cervical length will be assessed in all patients, once abdominally and then vaginally (that would serve as golden standard). Correlation would be assessed between accuracy of measurement to BMI

NCT ID: NCT01881698 Recruiting - Pregnancy Clinical Trials

Evaluation of Platelet Function in Pregnancy With Multiple Electrode Aggregometry

MULPP
Start date: October 2013
Phase: N/A
Study type: Observational [Patient Registry]

Establishment of a range of normal values in pregnancy with the Multiple Electrode Aggregometry (Multiplate@) device, a device that allows measurement of not only platelet count but platelet function. This has not been studied in ths special patient group. Results from this trial will be used as a basis for further investigation of abnormal platelet function in pregnancy.

NCT ID: NCT01875172 Completed - Pregnancy Clinical Trials

Bupropion for Smoking Cessation in Pregnancy

Start date: October 2001
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether bupropion SR increases cessation and/or smoking reduction among pregnant smokers.

NCT ID: NCT01868074 Active, not recruiting - Pregnancy Clinical Trials

Study of Changes in the Feet With Pregnancy

Start date: May 2013
Phase: N/A
Study type: Interventional

This research is being conducted to determine whether use of an arch-supporting insole during pregnancy prevents alterations in foot structure and lower limb rotational movements. The investigators hypothesize that the arch collapse during pregnancy will be significantly reduced in women randomized to use the supportive insole compared with women randomized to the control group.

NCT ID: NCT01865955 Completed - Pregnancy Clinical Trials

Comparison Between Palpatory and Preprocedural Ultrasound Guided Techniques on Performance of Spinal Anesthesia

Start date: May 2013
Phase: N/A
Study type: Interventional

Pre-procedural ultrasound for Spinal & Epidural anesthesia is now being increasingly performed worldwide. Pre-procedural ultrasound assessment of the spine has been shown to facilitate the placement of epidural anesthesia in pregnant women, diagnostic lumbar punctures, performance of spinal anesthesia in non-obstetric patients and accurate identification of the interspace at which the puncture is being performed. This is especially important during spinal anesthesia, where puncture below the ending of the spinal cord is recommended for safety. The purpose of this study is to compare the performance of spinal anesthesia between the pre-procedural ultrasound assessment of the spine and the traditional palpatory technique, in term pregnant women undergoing elective cesarean delivery. Furthermore, we aim to describe sonoanatomic features of the spine that could predict the ease of insertion of spinal anesthesia in that patient population. We hypothesize that in term pregnant women undergoing elective cesarean delivery, pre-procedural ultrasound assessment of the spine will improve the success rate of spinal anesthesia at first attempt, compared to the traditional palpatory technique.

NCT ID: NCT01865136 Completed - Pregnancy Clinical Trials

Post-abortion Care and Contraceptive Counselling by Midwives or Physicians

Start date: September 2013
Phase: Phase 4
Study type: Interventional

The aim of this project is to study the safety, efficacy and effectiveness of medical treatment of incomplete abortion provided to women by physicians or midwives in Kisumu, Kenya. In Kenya, Post Abortion Care (PAC), provided by physicians, nurse-midwives and clinical officers, has been integrated at private reproductive health facilities since 1998. Misoprostol as treatment of incomplete abortion was launched I Nyanza Province in April, 2012. The involvement of midwives in medical (Misoprostol) treatment of incomplete abortion has, however, not been systematically evaluated. There is a need to determine whether midwives and physician can perform medical treatment of incomplete abortion equally safe and effective in Kenya. The results will thus provide evidence-based information that can contribute to the development of strategies to increase women's access to Post Abortion Care in Kenya as well as in other low-income contexts.

NCT ID: NCT01863446 Active, not recruiting - Pregnancy Clinical Trials

Effects of Light on Melatonin and Contractions in Pregnant Women

Start date: May 2013
Phase: N/A
Study type: Interventional

Specific Aim: Test the hypothesis that ocular light exposure will suppress melatonin secretion and reduce uterine contractions in women at late term pregnancies. Secondary aim. Test the hypothesis that ocular light exposure will reduce self-reported uterine contractions in women at late term pregnancies.

NCT ID: NCT01857310 Completed - Pregnancy Clinical Trials

Folic Acid and Zinc Supplementation Trial (FAZST)

FAZST
Start date: June 2013
Phase: N/A
Study type: Interventional

The overarching goal of this trial is to determine if an intervention comprising folic acid and zinc dietary supplementation improves semen quality and indirectly fertility outcomes (i.e., live birth rate) among couples trying to conceive and seeking assisted reproduction. The following study objectives underlie successful attainment of the overarching research goal: 1. To estimate the effect of folic acid and zinc dietary supplementation on semen quality parameters, including but not limited to concentration, motility, morphology, and sperm DNA integrity, relative to the placebo group. 2. To estimate the effect of folic acid and zinc dietary supplementation on fertility treatment outcomes [fertilization, embryo quality, implantation/human Chorionic Gonadotropin (hCG) confirmed pregnancy, clinical pregnancy, live birth], relative to the placebo group. 3. To estimate the association between semen quality parameters, sperm DNA integrity and fertility treatment outcomes (fertilization, embryo quality, clinical pregnancy, live birth) and to identify the best combination of semen quality parameters for prediction of clinical pregnancy and live birth. 4. To estimate the effect of folic acid and zinc dietary supplementation on fertilization rates among couples undergoing assisted reproductive technology procedures, relative to the placebo group. 5. To estimate the effect of folic acid and zinc dietary supplementation on embryonic quality among couples undergoing assisted reproductive technology procedures, relative to the placebo group.

NCT ID: NCT01856166 Completed - Pregnancy Clinical Trials

PIEB-PCEA Versus CEI-PCEA for Labor Analgesia in Nulliparous

PIEB
Start date: June 2013
Phase: N/A
Study type: Interventional

Epidural analgesia still have an impact on obstetric outcomes and especially on instrumented delivery rates. To assess the best maintainance regimen of epidural analgesia during labor the investigators plan to include 300 nulliparous in this multicenter randomized, double blind trial. The primary outcome will be a composite set of criteria that can lead to instrumented delivery. Secondary outcome will focus on analgesia motor block and satisfaction.

NCT ID: NCT01855763 Active, not recruiting - Type 2 Diabetes Clinical Trials

Metformin Treatment in Gestational Diabetes and Noninsulin Dependent Diabetes in Pregnancy in a Developing Country

migdm&t2dm
Start date: December 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The study hypothesis was In women with gestational diabetes and type 2 diabetes in pregnancy metformin treatment compared with insulin will result in better perinatal and maternal outcome and improved treatment acceptability with low or noadditional insulin requirement.