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Labor clinical trials

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NCT ID: NCT00840710 Not yet recruiting - Labor Clinical Trials

Clinical Feasibility of Birth- Track II System

BT
Start date: February 2010
Phase: N/A
Study type: Observational

The Study purpose is to monitor the cervix dilation, head descent, FHR and to follow contraction in a women in active labor.

NCT ID: NCT00827229 Completed - Labor Clinical Trials

Evaluation of Laborpro - a New Device for the Assessment of Progress of Labor

Start date: January 2007
Phase: N/A
Study type: Interventional

A clinical study was conducted to demonstrate the accuracy of the LaborPro System in measuring fetal head station (from the pelvic inlet), cervical dilatation, and fetal head position against manual/digital examination. The LaborPro obtained device values was compared to measurements gathered within 15 minutes by manual/digital examination performed by two independent physicians. The study was a non significant risk (NSR) device study.

NCT ID: NCT00827125 Recruiting - Pregnancy Clinical Trials

Determination of Labor Progression Patterns Using Non-invasive, Ultrasound Based, Multiple Parameters

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to establish normograms of parameters measured by the LaborPro system. To test the prediction of these parameters on labor progress and mode of delivery.

NCT ID: NCT00801047 Completed - Pain Clinical Trials

Intravenous Remifentanil Patient-controlled Analgesia (PCA) and Epidural Patient Controlled Epidural Analgesia (PCEA) for Labor Analgesia

Start date: February 2010
Phase: Phase 4
Study type: Interventional

Women requesting analgesia do not always wish to receive a potent analgesic method, and may fear the risks of epidural analgesia. Study Aim: To determine whether remifentanil is effective for labor analgesia when compared with standard treatment (epidural analgesia).

NCT ID: NCT00710242 Completed - Pregnancy Clinical Trials

Study to Assess Safety and Efficacy of DF01 in Reducing Prolonged Labor

Start date: April 2007
Phase: Phase 2
Study type: Interventional

The study is a Proof-of-concept study to evaluate if DF01 can prevent protracted labor. Time to delivery will be measured from the time of at least 3 cm cervix dilatation and 3 contractions of minimum one minute's duration/10 minutes.

NCT ID: NCT00695331 Recruiting - Labor Clinical Trials

Efficacy and Safety Study of Titrated Oral Misoprostol Solution for Labor Augmentation

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

The purpose of this study is to compare the efficacy and safety of titrated oral misoprostol solution with intravenous oxytocin for labor augmentation in women without adequate uterine contractions.

NCT ID: NCT00665405 Completed - Cesarean Section Clinical Trials

Atelectasis During Delivery - Comparing Cesarian (c) -Section and Labor

Start date: July 2006
Phase: N/A
Study type: Observational

Pregnancy promotes respiratory system's restrictive component. This study observes the generation of atelectasis during labor.

NCT ID: NCT00569439 Completed - Labor Clinical Trials

A Study on the Effects of Dextrose Solutions on the Course of Labor

Start date: November 2000
Phase: Phase 2
Study type: Interventional

The purpose is to determine in term nulliparas with singletons that present in active labor (3-5 cm) or with ruptured membranes whether the administration of dextrose solutions to normal saline improves or expedites the course of labor. The researchers' hypothesis is that the addition of a carbohydrate substrate will shorten the length of labor and facilitate a vaginal delivery.

NCT ID: NCT00502918 Terminated - Labor Clinical Trials

Clinical Feasibility of Computerized Labor Monitor (CLM) -Heart Application (HA)

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

The study is a feasibility study to check the possibility of tracking the heart rate of the fetus and to translate the outcome to the progress of the labor

NCT ID: NCT00496899 Terminated - Labor Clinical Trials

Clinical Evaluation of New Computerized Labor Monitoring System

CLM
Start date: June 2007
Phase: N/A
Study type: Observational

The study is an open label feasibility study. The purpose of the study is to evaluate the ease of use of the Cervical ITR in terms of duration of attachment and number of detachments.