Other Clinical Trial - Evaluate the Efficacy & Safety of MEDITOXIN in

See also
Status	Clinical Trial	Phase
Completed	`NCT05057117` - Longevity of Microwave Thermolysis and Botulinum Toxin A for Treatment of Axillary Hyperhidrosis	Phase 4
Recruiting	`NCT05860972` - Evaluation of Safety and Efficacy of Morpheus8 Applicator for the Treatment of Focal Hyperhidrosis of the Axillae Using Radio Frequency	N/A
Enrolling by invitation	`NCT04227691` - Treatment of Axillary Hyperhidrosis With Long-pulsed Nd:YAG Laser or IPL	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT05057117 - Longevity of Microwave Thermolysis and Botulinum Toxin A for Treatment of Axillary Hyperhidrosis

Phase 4

Recruiting

NCT05860972 - Evaluation of Safety and Efficacy of Morpheus8 Applicator for the Treatment of Focal Hyperhidrosis of the Axillae Using Radio Frequency

N/A

Enrolling by invitation

NCT04227691 - Treatment of Axillary Hyperhidrosis With Long-pulsed Nd:YAG Laser or IPL

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03760198
Study type	Interventional
Source	Medy-Tox
Contact
Status	Completed
Phase	Phase 3
Start date	August 3, 2018
Completion date	September 17, 2019

Evaluate the Efficacy and Safety of MEDITOXIN in Treatment of Primary Axillary Hyperhidrosis

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms