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Clinical Research Directory

Browse clinical research sites, groups, and studies.

4 clinical studies listed.

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Myotonia

Tundra lists 4 Myotonia clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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ENROLLING BY INVITATION

NCT06492057

Electromyostimulation (EMS) of Astronauts in Spaceflight (Easymotion-2)

This is a prospective spaceflight study involving an investigational non-risk device called the EasyMotionSkin for whole body electric muscle (myo) stimulation (WB-EMS) onboard the International Space Station (ISS). The purpose of this study is to show: * optimized exercise outcome with EMS in human spaceflight * demonstrate efficacy of EMS as alternative inflight exercise protocol * provide a time-saving and reliable EMS-assisted exercise protocol compliant to astronauts for later use in planetary habitats and future deep space exploration Eight (n=8) astronauts on long duration missions will take part in this study. This experiment uses the following hardware/software (HW \& SW): (A) EasymotionSkin suit (dry electrode muscle stimulation), B) non-invasive hand-held Myoton device (digitized passive muscle stiffness data collection). C) a customized Myoton body template suit (elastic yoga suit with customized anatomical reference labels to aid inflight Myoton data collection on dedicated perforated 2x2 cm small skin fields) at 5 different skin measurement points (MP), neck, back, shoulder, legs. Before and after flight the following tests will be done once: Myoton data collection, dynamometry strength test, magnetic resonance imaging (MRI) for baseline comparison. Researchers will compare data from a non EMS control group (non EMS Astronauts, retrospective) to see if changes of passive muscle stiffness is seen in EMS Astronauts before, during and after spaceflight

Gender: All

Ages: 40 Years - 60 Years

Updated: 2026-03-23

1 state

Muscle Atrophy
Myotonia
Stiffness; Spine
+1
ENROLLING BY INVITATION

NCT07008469

Global Open-Label Extension Study of Del-desiran for the Treatment of DM1

A Global Phase 3 Open-Label Extension Study to Assess the Long-Term Safety, Tolerability, and Efficacy of Intravenous Delpacibart Etedesiran (abbreviated del-desiran, formerly AOC 1001) for the Treatment of Myotonic Dystrophy Type 1

Gender: All

Ages: 16 Years - Any

Updated: 2026-02-03

16 states

Myotonic Dystrophy Type 1
DM1
Myotonic Dystrophy
+5
ACTIVE NOT RECRUITING

NCT06411288

Global Study of Del-desiran for the Treatment of DM1

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Global Study to Evaluate the Efficacy and Safety of Intravenous Delpacibart Etedesiran (abbreviated del-desiran, formerly AOC 1001) for the Treatment of Myotonic Dystrophy Type 1

Gender: All

Ages: 16 Years - 65 Years

Updated: 2026-01-22

18 states

DM1
Myotonic Dystrophy
Myotonic Dystrophy 1
+7
RECRUITING

NCT07097701

An Open-Label, Randomized, Cross-Over Study to Investigate the Efficacy and Safety of Mexiletine PR Compared to Mexiletine IR

An Open-Label, Randomized, Cross-Over Study to Investigate the Efficacy and Safety of Mexiletine PR compared to Mexiletine IR in Patients with Non-Dystrophic Myotonias (ACHILLES study)

Gender: All

Ages: 16 Years - Any

Updated: 2025-12-22

Myotonia