Clinical Trials Directory

Trials / Completed

CompletedNCT05501444

Antiperspirant in the Treatment of Residual Limp Hyperhidrosis for Prosthetic Users

Antiperspirant in the Treatment of Residual Limp Hyperhidrosis for Prosthetic Users: a Pilot Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
7 (actual)
Sponsor
Sophies Minde Ortopedi · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the present pilot study is to evaluate the effect of antiperspirant to treat residual limb hyperhidrosis with the emphasis on the utility of the iodine-starch test to identify the location of the sweating.

Detailed description

Many persons with lower limb amputation report that they have major problems with sweating (hyperhidrosis) on the stump in connection with prosthetic use. Despite the frequency and the negative effect of sweating for prosthetic users, there is a lack of evidence on how the sweating should be examined and treated. In the dermatological literature, the guidelines recommend the use of topical antiperspirants such as aluminum chloride as first-line treatment. No studies have previously been published evaluating the effect of antiperspirant on prosthetic users.

Conditions

Interventions

TypeNameDescription
OTHERTopical antiperspirantThe participants will be instructed to use topical antiperspirant (aluminum chloride, 15 percent every evening for four weeks. The PI will contact the participants every week. If the participant experiences that antiperspirant have an effect, the use of antiperspirant will be reduced from daily use to 3 times a week.

Timeline

Start date
2022-08-09
Primary completion
2022-12-31
Completion
2023-03-30
First posted
2022-08-15
Last updated
2023-04-13

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT05501444. Inclusion in this directory is not an endorsement.