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Dystocia clinical trials

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NCT ID: NCT01618565 Completed - Shoulder Dystocia Clinical Trials

Objective Structured Assessment of Technical Skills (OSATS) Evaluation of Shoulder Dystocia Management

Start date: April 2012
Phase: Phase 3
Study type: Interventional

This trial tests whether hands-on training is superior to expert demonstration regarding the management of shoulder dystocia (stuck shoulder) during delivery on a training model.

NCT ID: NCT01530113 Not yet recruiting - Depression Clinical Trials

Childhood Sexual Abuse, Vaginismus and Labor Dystocia

CSA-V-LD
Start date: March 2012
Phase: N/A
Study type: Observational

The study aims to develop a theoretical model explicating the inter-relationships between Childhood Sexual Abuse (CSA), Partial Vaginismus (PV) and Labor Dystocia (LD), including their associations with Depression (D) as a mediating variable. The following research hypotheses will be tested: 1. CSA will serve as a risk factor for D, PV and LD. - pregnant women with a history of CSA will have higher levels of D compared to pregnant women without a history of CSA. - pregnant women with a history of CSA will have more PV compared to pregnant women without a history of CSA. - pregnant women with a history of CSA will have higher levels of LD compared to pregnant women without a history of CSA. 2. D will serve as a mediator between prenatal PV and LD. 3. PV will serve as a risk factor for LD. 4. postpartum PV will be affected by childbirth (LD vs. no LD) contingent on the level of D.

NCT ID: NCT01397630 Terminated - Labour Dystocia Clinical Trials

Accelerated Titration of Oxytocin for Nulliparous Patients With Labour Dystocia: ACTION Pilot Study

ACTION
Start date: April 2012
Phase: Phase 3
Study type: Interventional

The ultimate objective is to test the hypothesis that an 'accelerated titration' protocol for labour augmentation with oxytocin reduces the risk of caesarean births relative to a 'gradual titration' protocol. The aims of this pilot feasibility are: 1. To assess the feasibility of a large multi-centre randomized control trial comparing the two above oxytocin protocols (accelerated titration versus gradual titration for correction of dystocia). 2. More specifically, to identify potential challenges in the study implementation, particularly with respect to patient recruitment, randomization, blinding, and compliance/adherence to the labour management guidelines and study protocols. 3. To obtain preliminary data on the acceptability of the accelerated oxytocin titration protocol among obstetrical providers and participants.

NCT ID: NCT01297439 Terminated - Clinical trials for Brachial Plexus Injury

New Prophylactic Maneuver: the "Pushing" Maneuver, Aiming to Reduce the Risk for Shoulder Dystocia

CONTRADYS
Start date: March 2011
Phase: N/A
Study type: Interventional

Shoulder dystocia is a major obstetric emergency defined as a delivery requiring maneuver in addition to downward traction on the fetal head for delivery of the shoulders. Shoulder dystocia is a major obstetrical complication, occurring in approximately 0.2 to 3% of deliveries, principally due to fetal macrosomia. The obstetrical and neonatal complications associated with shoulder dystocia include newborn mortality occurring in 21 to 290 per 1000 deliveries, generalized asphyxia, fractures, neurological damages (brachial plexus injury) and hematoma. The objective of this study was to evaluate the "pushing" maneuver, that is performed gently on the fetal head since the crowning of the head (appearance of the fetal scalp at the introitus between pushes), aiming to facilitate the anterior shoulder to slip off behind the symphysis pubis, reducing thus the risk of shoulder dystocia. This preventive maneuver may reduce the power (energy/time unit) exerted on the perineal tissues and give the shoulders time to enter the pelvic cavity. The "pushing" maneuver will be evaluated in comparison with either an expectative attitude or a suctioning of fetal nose and mouth.

NCT ID: NCT01291355 Completed - Dystocia Clinical Trials

Maternal Positioning and Occipitoposterior Fetal Position

Start date: February 2011
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the efficacy of a specific maternal position to correct fetal position in occipito-posterior during the labor. The investigators hypothesize that the maternal position described by the Dr de Gasquet facilitate the rotation in occipito-anterior during the labor. The calculated sample size is 438 participants (219 in each group)

NCT ID: NCT01107158 Terminated - Dystocia Clinical Trials

LXRs, Cholesterol Metabolism and Uterine Dystocia

Start date: April 2010
Phase: N/A
Study type: Observational

Despite the fact that a link between cholesterol and the myometrium has been clearly established, no study investigating aspects of cholesterol metabolism and uterine dystocia currently exists. This study is a pilot study whose aim is to test the hypothesis that an association between uterine dystocia and single-nucleotide polymorphisms (SNPs) in the genes coding for the LXRs.

NCT ID: NCT00481533 Completed - Clinical trials for Blood Loss, Surgical

Ergot and Oxytocin During Cesarean Delivery Following Failure to Progress in Labour

Start date: June 2005
Phase: N/A
Study type: Interventional

Despite of marked improvements in clinical management, early postpartum hemorrhage(PPH)remains a significant contributor to maternal morbidity and mortality both in developing countries and in hospitals equipped with all that modern medicine has to offer. This complication is amongst the most challenging that a clinician will face in the obstetric patient. Prevention, early recognition and prompt appropriate intervention are the keys to minimizing the impact of PPH on women’s health. Patients undergoing Cesarean sections following failure to progress in labor are at great risk for PPH and should theoretically benefit from an additional uterotonic agent. This study will be conducted to define whether the addition of ergonovine maleate to oxytocin, administered in a prophylactic way, reduces blood loss during Cesarean section for failure to progress in labor.

NCT ID: NCT00315913 Withdrawn - Dysfunctional Labor Clinical Trials

Trial of Oxytocin Alone Versus Oxytocin and Propranolol for the Treatment of Abnormal Labor

Start date: January 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether propranolol is better than oxytocin for the treatment of labor abnormalities. The endpoint is the rate of vaginal delivery experienced by women receiving prolonged oxytocin versus propranolol.

NCT ID: NCT00279071 Terminated - Dystocia Clinical Trials

Use of Acupuncture for Stimulation of Labour

Start date: October 2002
Phase: Phase 2
Study type: Interventional

Hypothesis:Acupuncture can be used as stimulation of labour in case of primary og secondary inertia. A randomized controlled trial including 150 pregnant women Acupuncture has become a natural part of the range of obstetric treatments offered in danish delivery wards, but there is only little evidence to the effect of the acupuncture. The women are randomized into to groups. 1. Acupuncture, Acu.points: KI3, Ki6, SP6, BL60, LI4, BL67(acupressure) 2. No treatment The women will be asked in case beginning signs of inertia, if they want to parcipitate in the trial. Inclusion criteria: 1. Normal pregnancy 2. In labour (orificium < 8 cm), 37th week or thereafter 3. Ruptured membranes 4. Primary or secondary inertia The women will just before randomization be vaginally explored and fetal heart monitored. The meassure of effect happens two hours after randomization. The midwife who measures the effect, is blinded to the treatment or lack of, and also on the including exploration. Secondary effect meassures: length of labour, use of oxytocin and number of contracions pr/min meassured twice: 1. before the randomization and again 1 hour after randomization.