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Congenital Abnormalities clinical trials

View clinical trials related to Congenital Abnormalities.

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NCT ID: NCT05494710 Recruiting - Clinical trials for Vascular Malformations

Bleomycin Electrosclerotherapy Treatment of Vascular Malformations: A Feasibility Study

BEST
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The aim of the BEST study is to examine the feasibility of assessing patient and clinician reported outcome of a single electrosclerotherapy treatment of vascular malformations. - Sclerotherapy = injection of Bleomycin into vascular birthmarks to seal off abnormal vascular channels - Electroporation = application of an electric field to vessels treated with a handheld needle electrode - Electrosclerotherapy = a combination of Bleomycin sclerotherapy and electroporation

NCT ID: NCT05492708 Recruiting - Pregnancy Related Clinical Trials

The Heartland Study

Start date: January 11, 2020
Phase:
Study type: Observational

The Heartland Study is a prospective, observational study that will enroll up to 2,600 pregnant participants across the Heartland States in the U.S.. The objective of the Heartland Study is to address major knowledge gaps concerning the health effects of herbicides on maternal and infant health. The study is being conducted to evaluate the associations between environmental exposures to herbicides during and after pregnancy and reproductive health outcomes. The study is measuring multiple biomarkers of herbicide exposure among pregnant Midwesterners and their partners to evaluate associations with pregnancy and childbirth outcomes, epigenetic biomarkers of exposure, and child development.

NCT ID: NCT05491343 Not yet recruiting - Clinical trials for Arteriovenous Malformations

Observation vs Progesterone Treatment for Management of Uterine Arteriovenous Malformation

Start date: August 2022
Phase: Phase 4
Study type: Interventional

A randomized trial which compares conservative management to progesterone based treatment for arteriovenous malformation

NCT ID: NCT05489315 Recruiting - Labor Long Clinical Trials

Quantifying the Impact of the Peanut Ball on the Duration of the Active Stage of Labor

Start date: July 26, 2021
Phase: N/A
Study type: Interventional

Prolonged labor is associated with adverse maternal and fetal outcomes including infection, postpartum hemorrhage and increased NICU admission. One of the most common indications for cesarean section in the US is prolonged labor. Maternal positioning through labor facilitated by birthing balls is believed to help facilitate labor. Current data is inconclusive on whether or not the use of birthing balls is advantageous in a statistically significant manner. In this prospective randomized controlled trial, participants will be randomly selected to receive either the experimental intervention (repositioning peanut ball during labor) or the control intervention (the standard therapy of traditional repositioning during labor). Primary outcome: Time of active labor to delivery with and without use of the peanut ball. Secondary outcome: Cesarean section frequency.

NCT ID: NCT05484934 Recruiting - Clinical trials for Post-Mastectomy Breast Deformity (Disorder)

Investigate Wound Healing, Aesthetics & Pt Satisfaction Post NAC Reconstruction Using a Decellularized Donor NAC Graft

Start date: September 21, 2022
Phase: N/A
Study type: Interventional

To evaluate the wound healing response following nipple-areolar complex (NAC) reconstruction with a decellularized donor NAC graft (DCLNAC)

NCT ID: NCT05484596 Recruiting - Clinical trials for Pulmonary Vascular Resistance Abnormality

PV Loop and Pulmonary Hypertension

Start date: April 27, 2020
Phase:
Study type: Observational

The right ventricular (RV) systolic function is a key determinant of outcome in patients with pulmonary hypertension and elevated pulmonary vascular resistance. As the pulmonary artery pressure and vascular resistance increase (i.e. RV afterload) in these patients, so does the right ventricular contractility in an attempt to maintain cardiac output. This is response of a ventricle to its afterload is termed ventriculo-arterial (VA) coupling. However, there is a limit to this increase in contractility after which VA uncoupling occurs ultimately leading to decrease cardiac output and right ventricular failure. The accepted gold standard for measurement of VA coupling is the ratio of the end systolic ventricular elastance (Ees) to the end systolic arterial elastance (Ea) measured invasively via high fidelity conductance catheters during cardiac catheterization. In this study, the aim is to devise a non-invasive scoring system that can identify VA uncoupling in patients with elevated pulmonary vascular resistance using echocardiography, cardiac MRI, cardiopulmonary exercise testing and brain natriuretic peptide levels. The hypothesis is that a group of morphologic and functional variables obtained noninvasively can differentiate an RV with VA coupling from that with VA uncoupling.

NCT ID: NCT05484362 Completed - Blood Pressure Clinical Trials

Acute Effect of Crocus Sativus on Postprandial Glycemia

Start date: June 6, 2022
Phase: N/A
Study type: Interventional

This study investigated the effects of two different doses of Crocus Sativus in glucose beverages on glycemic responses.

NCT ID: NCT05484336 Completed - Blood Pressure Clinical Trials

Acute Effects of Spirulina on Postprandial Glycemic Responses and Arterial Blood Pressure

Start date: June 7, 2022
Phase: N/A
Study type: Interventional

This study investigated the effects of three doses of spirulina in glucose beverages on postprandial glycemic responses, arterial blood pressure, and subjective satiety.

NCT ID: NCT05484323 Completed - Blood Pressure Clinical Trials

Acute Effects of Cookies Containing 2.5 g Spirulina on Postprandial Glycemic and Insulin Responses

Start date: January 15, 2022
Phase: N/A
Study type: Interventional

This study investigated the effects of cookies containing 2.5 g Spirulina on postprandial glycemic and insulin responses.

NCT ID: NCT05484245 Recruiting - Clinical trials for Arteriovenous Malformations

Sonography-guided Resection of Brain Mass Lesions

SOMALI
Start date: September 1, 2022
Phase: N/A
Study type: Interventional

Objective of the study is to determine possibilities of intraoperative sonography in detecting of various brain mass lesions, assessing extent of their resection and define indications to use ultrasound-guided needle or ultrasound wire-guided port.