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Arthrogryposis clinical trials

View clinical trials related to Arthrogryposis.

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NCT ID: NCT05401409 Completed - Hypertension Clinical Trials

Effect of Beetroot Juice on Reducing Hypertension in Autosomal Dominant Polycystic Kidney Disease

BEET-PKD
Start date: May 5, 2022
Phase: N/A
Study type: Interventional

People with autosomal dominant polycystic kidney disease (ADPKD) develop high blood pressure and kidney disease. Previous studies have shown that a commonly occurring chemical, nitric oxide (NO), is reduced in ADPKD, and may contribute, in part, to high blood pressure in this condition. Nitrate is found in high concentrations naturally in beetroots, and increases NO. The aim of this study is to determine if beetroot juice reduces blood pressure in hypertensive people with ADPKD.

NCT ID: NCT05393375 Completed - Pediatric ALL Clinical Trials

Arthrogryposis Multiplex Congenita in Pediatric Age: Correlation Between MUScular MRI and Functional Evaluation

AMUSE
Start date: May 1, 2022
Phase:
Study type: Observational

The aim of our study is to evaluate the correlation between quantified fibro-adipous infiltration of muscles on MRI assessed by MERCURI Score and the functional abilities (deficiencies, activity limitations and social participation of pediatric patients with arthrogryposis.

NCT ID: NCT05137756 Completed - Clinical trials for Diagnosis of Arthrogryposis Amyoplasia or Distal Arthrogryposis

Mercuri Analysis Contribution on Handicap Evaluation in ArthrogypOsis, a Congenital Neuromuscular Disease

MACHAON
Start date: December 1, 2019
Phase:
Study type: Observational

The aim is to evaluate the correlation of quantified fibro-adipous infiltration of muscles, using the MRI-based Mercuri score, with deficiencies, activity limitations and social participation in patients with arthrogryposis multiplex congenita.

NCT ID: NCT04581629 Completed - Clinical trials for Autosomal Dominant Hypocalcemia (ADH)

Safety, Tolerability, and Efficacy of Encaleret in Participants With Autosomal Dominant Hypocalcemia (ADH) Type 1

Start date: September 15, 2020
Phase: Phase 2
Study type: Interventional

The primary purpose of this study is to evaluate the safety, tolerability and effectiveness of encaleret in participants with Autosomal Dominant Hypocalcemia Type 1 (ADH1).

NCT ID: NCT04536688 Completed - Clinical trials for Polycystic Kidney Disease, Autosomal Dominant

A Study of RGLS4326 in Patients With Autosomal Dominant Polycystic Kidney Disease

Start date: October 13, 2020
Phase: Phase 1
Study type: Interventional

Primary Objective • To assess the dose response relationship between RGLS4326 and ADPKD biomarkers Secondary Objectives - To characterize the pharmacokinetic (PK) properties of RGLS4326 in plasma and urine - To assess the safety and tolerability of RGLS4326

NCT ID: NCT04534985 Completed - Clinical trials for Polycystic Kidney, Autosomal Dominant

Time Restricted Feeding in Autosomal Dominant Polycystic Kidney Disease

Start date: February 9, 2021
Phase: N/A
Study type: Interventional

The proposed research will determine the feasibility of a time restricted feeding intervention,a fasting regimen that restricts eating to a feeding window (8 hrs/day) for 1 year in adults with autosomal dominant polycystic kidney disease (ADPKD) who are overweight or obese. The study will provide valuable information on the intervention in terms of safety, adherence, acceptability, and tolerability. Last, this pilot trial will provide initial insight into biological changes including abdominal adiposity, changes in kidney growth and function, and markers of biological pathways related to the intervention.

NCT ID: NCT03949894 Completed - Clinical trials for Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Evaluating the Safety and effectivenesS in Adult KorEaN Patients Treated With Tolvaptan for Management of Autosomal domInAnt poLycystic Kidney Disease

ESSENTIAL
Start date: July 1, 2019
Phase: Phase 4
Study type: Interventional

To evaluate the safety and therapeutic effectiveness of tolvaptan when administered to slow the progression of cyst development and renal function insufficiency in adult Korean patients diagnosed with rapidly progressive ADPKD who have chronic kidney disease (CKD) stages 1-3 at initiation of treatment.

NCT ID: NCT03487913 Completed - Clinical trials for Autosomal Dominant Polycystic Kidney Disease

The ELiSA Study - Evaluation of Lixivaptan in Subjects With Autosomal Dominant Polycystic Kidney Disease

Start date: September 14, 2018
Phase: Phase 2
Study type: Interventional

This is a Phase 2, open-label, parallel-group, multiple dose study designed to evaluate the pharmacokinetics, pharmacodynamics, safety and tolerability of multiple doses of lixivaptan in Autosomal Dominant Polycystic Kidney Disease subjects with chronic kidney disease (CKD) in stages CKD1, CKD2 or CKD3.

NCT ID: NCT03342742 Completed - Clinical trials for Polycystic Kidney, Autosomal Dominant

Daily Caloric Restriction and Intermittent Fasting in Overweight and Obese Adults With Autosomal Dominant Polycystic Kidney Disease

Start date: June 4, 2018
Phase: N/A
Study type: Interventional

The proposed research will determine the feasibility of delivering two behavioral weight loss interventions for 1 year in adults with autosomal dominant polycystic kidney disease (ADPKD) who are overweight or obese. The study will also compare these two interventions in terms of safety, acceptability, and tolerability. Last, this pilot trial will provide initial insight into a) biological changes and b) changes in kidney growth with each of the two weight loss interventions.

NCT ID: NCT03203642 Completed - Clinical trials for Autosomal Dominant Polycystic Kidney

Study of the Efficacy and Safety of Tesevatinib in Subjects With ADPKD

Start date: October 12, 2017
Phase: Phase 2
Study type: Interventional

The goal of the study was to compare and evaluate safety and efficacy of tesevatinib 50 milligrams (mg) versus placebo in participants with autosomal dominant polycystic kidney disease (ADPKD).