Completed OBSERVATIONAL NCT02380729

Mutation Exploration in Non-acquired, Genetic Disorders and Its Impact on Health Economy and Life Quality (MENDEL)

Sponsor: Charite University, Berlin, Germany

Interventions Gene Panel Sequencing Whole Genome Sequencing (WGS)

Updated 11 times since 2017 Last updated: Jan 24, 2018 Started: Jan 31, 2015 Primary completion: Jun 30, 2017 Completion: Dec 31, 2017

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A observational or N/A phase clinical study on Genetic Diseases, this trial is completed. The trial is conducted by Charite University, Berlin, Germany and has accumulated 11 data snapshots since 2015. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

11 versions recorded

Sep 2024 — Present [monthly]

Completed
Jul 2024 — Sep 2024 [monthly]

Completed
Dec 2021 — Jul 2024 [monthly]

Completed
Jan 2021 — Dec 2021 [monthly]

Completed
Nov 2020 — Jan 2021 [monthly]

Completed

▶ Show 6 earlier versions

Jun 2018 — Nov 2020 [monthly]

Completed
May 2018 — Jun 2018 [monthly]

Completed
Apr 2018 — May 2018 [monthly]

Completed

Phase: NA → None
Feb 2018 — Apr 2018 [monthly]

Completed NA

Status: Recruiting → Completed
Aug 2017 — Feb 2018 [monthly]

Recruiting NA
Jan 2017 — Aug 2017 [monthly]

Recruiting NA

First recorded

Jan 2015

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Charite University, Berlin, Germany
German Federal Ministry of Education and Research

Data source: Charite University, Berlin, Germany

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Berlin, Germany