Clinical trials

2

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

AV Node Ablation and CONDUCTion System Pacing for Atrial Fibrillation With Preserved Left Ventricular Function

AVA CONDUCT is a prospective, multicenter, randomized study with single blinding, comparing left bundle branch area (LBBA) pacing with right ventricular (RV) pacing following AV node ablation in terms of clinical, functional, and electrophysiological outcomes. The primary hypothesis is that pacing-induced cardiomyopathy, defined as a decrease in LVEF by 10% or more from baseline to an absolute value below 50%, occurs significantly more frequently in patients receiving RV pacing compared with LBBA pacing. Secondarily, LBBA pacing is expected to maintain comparable procedural safety while providing better cardiac function, resulting in improved quality of life and functional capacity compared with conventional RV pacing.

Participants needed: 86
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: St. Josefs-Hospital Wiesbaden GmbHUpdated: Feb 24, 2026Locations: 2
Eligibility criteria

History of symptomatic AF (EHRA IIb - IV) despite guideline-indicated medical or... [+4]

Impaired LVEF (< 50%) [+8]

Status: Recruiting

Evaluation of the Subjectively Perceived Pelvic Floor Function in Patients With Gynecological Tumors and Breast Cancer Under Systemic Tumor Therapy Using a Validated Questionnaire

The multimodal therapy of gynecological malignancies and breast cancer often leads to an impairment of the pelvic floor function. This has a major impact on the quality of life of cancer patients. The aim of the study is to record and analyze the potential subjective impairment of the bladder, bowel and sexual function under systemic tumor therapy as well as possible influencing factors by means of validated disease-specific questionnaires. to find possible starting points for the prevention and treatment of the symptoms.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: St. Josefs-Hospital Wiesbaden GmbHUpdated: Sep 23, 2025Locations: 1Duration: 3 Years
Eligibility criteria

Breastcancer under tumor therapy [+1]

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