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PREPL in Health and Disease

NCT02263781 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 125

Last updated 2024-07-16

No results posted yet for this study

Summary

Evaluation of PREPL activity in healthy controls and known or possible PREPL deficient patients

Conditions

Interventions

PROCEDURE

Blood draw

Blood draw

PROCEDURE

muscle biopsy

Muscle biopsy during planned anesthesia/surgery

Sponsors & Collaborators

  • KU Leuven

    collaborator OTHER

  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Principal Investigators

  • Luc Régal, MD · KU Leuven

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2025-01-31
Completion
2025-01-31

Countries

  • Belgium

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02263781 on ClinicalTrials.gov