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NCT ID: NCT05275257 Withdrawn - Clinical trials for Urinary Incontinence

Can the Use of Uricap Female Device Lead to Better Care for Women > 75+Years?

U-PROTECT
Start date: April 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate if Uricap Female, an uridome for women, can be used instead of traditional incontinence aids to treat urinary incontinence (UI) among women 75 years and older.

NCT ID: NCT05292976 Withdrawn - Bronchial Asthma Clinical Trials

Pharmacodynamic Bioequivalence Study of Albuterol Sulfate Inhalation Aerosol, 0.09 mg Albuterol Base/ Inhalation

Start date: April 2022
Phase: Phase 3
Study type: Interventional

Pharmacodynamic bioequivalence study of Albuterol Sulfate Inhalation Aerosol 0.09 mg

NCT ID: NCT05301595 Withdrawn - Breast Cancer Clinical Trials

TAP vs QL for Postoperative Analgesia After DIEP Free Flap Breast Reconstruction

Start date: April 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of Transversus abdominus plane (TAP) block and Quadratus Lumborum (QL) block on the quality of recovery after breast reconstruction with deep inferior epigastric perforator (DIEP) flap.

NCT ID: NCT05312021 Withdrawn - Clinical trials for Heart Failure With Preserved Ejection Fraction

Selective PDE9 Inhibition With IMR-687 in Adults With Heart Failure With Preserved Ejection Fraction

SP9In-HFpEF
Start date: April 2022
Phase: Phase 2
Study type: Interventional

This study is to evaluate whether 16 weeks of treatment with IMR-687 is a safe and effective treatment for patients with Heart Failure with Preserved Ejection Fraction (HFpEF). The primary objective is to evaluate whether IMR-687 reduces NT-proBNP compared to placebo in these patients.

NCT ID: NCT05578508 Withdrawn - Crohn's Disease Clinical Trials

Stem Cells for the Treatment of Pouchitis

Start date: April 2022
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and feasibility of using allogeneic bone marrow derived mesenchymal stem cells (MSCs) to treat people with medically refractory Pouchitis.

NCT ID: NCT05654064 Withdrawn - Clinical trials for Minimally Invasive Fetoscopic Procedures

Comparing Fetoscopic Surgery Protocols

Start date: April 2022
Phase: N/A
Study type: Interventional

Determine surgeon and patient satisfaction with remifentanil-dexmedetomidine (REMI) and dexmedetomidine-fentanyl (DEX) sedation protocols in pregnant patients undergoing minimally invasive fetoscopic procedures

NCT ID: NCT02995382 Withdrawn - Clinical trials for Cubital Tunnel Syndrome

Health-Related Quality of Life in Cases of Cubital Tunnel Syndrome

Start date: April 2023
Phase: N/A
Study type: Interventional

This study aims to determine the Health Related Quality of life (HRQOL) (the physical, mental, emotional and social functioning) of patients with cubital tunnel syndrome following anterior intramuscular transposition, after one year.

NCT ID: NCT03761511 Withdrawn - Friedreich Ataxia Clinical Trials

Study of the Efficacy and Safety of Nicotinamide in Patients With Friedreich Ataxia

NICOFA
Start date: April 2023
Phase: Phase 2
Study type: Interventional

Friedreich ataxia is the most frequent early-onset autosomal recessive hereditary ataxia. It is caused by a pathological expansion of a GAA repeat in the first intron of the frataxin gene (FXN) and results in decreased levels of FXN protein. FXN deficiency results in a relentlessly progressive neurodegenerative condition which frequently presents around puberty. Patients gradually lose coordination, become dysarthric and are frequently wheel-chair bound as adolescents. There is no disease modifying therapy and many patients die prematurely of cardiomyopathy. It was subsequently found that the FXN gene is silenced at the chromatin level by the formation of heterochromatin and that this heterochromatin formation can be antagonized by histone deacetylase inhibitors (HDACi) (Chan et al., 2013). A recent proof-of-concept clinical study on ten patients with Friedreich ataxia demonstrated that FXN levels can be restored to those seen in asymptomatic carriers using the class III HDACi nicotinamide at a dose that is well tolerated by patients (Libri et al., 2014). Since carriers are asymptomatic, this degree of restoration of FXN expression might be expected to halt disease progression. Nicotinamide readily crosses the blood brain barrier and has previously been given at high doses for long periods to normal individuals without serious adverse effects (Gale et al., 2004; Knip et al., 2000). This study will be the first to provide clinical evidence for the efficacy and safety of nicotinamide in patients with Friedreich´s ataxia.

NCT ID: NCT03982030 Withdrawn - Clinical trials for Gram-Positive Bacterial Infections

Dalbavancin Outpatient Pilot

Start date: April 2023
Phase: Phase 4
Study type: Interventional

The purpose of this research is to determine if a new antibiotic called dalbavancin will work to treat and cure certain infections while reducing the need for daily antibiotics by vein.

NCT ID: NCT04192019 Withdrawn - Type 1 Diabetes Clinical Trials

Micro Glucagon During Exercise in Type 1 Diabetes

Start date: April 2023
Phase: Early Phase 1
Study type: Interventional

This proof-of-principle study to assess effects of different doses (mini and micro) of subcutaneous glucagon analog Dasiglucagon (Zealand Pharma, Copenhagen, Denmark) on the change in blood glucose concentration during moderate-intensity exercise in people with T1D.