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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02758470
Other study ID # H16-00896
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date November 2016
Est. completion date June 30, 2017

Study information

Verified date September 2018
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this research is to assess the effects of acetazolamide and methazolamide on respiratory and limb muscle fatigue development. A fatiguing protocol will be conducted for the respiratory and plantar flexor muscles and the difference in pressure/torque produced by supramaximal nerve stimulation used to assess muscle fatigue between conditions.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date June 30, 2017
Est. primary completion date June 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Age: 18-40 years.

- Regularly physically active

- Male

Exclusion Criteria:

- current or ex-smokers

- pulmonary function <80% of predicted

- esophageal tumour or ulcer

- have had recent (<6 months) musculoskeletal injury or any surgery to the lower leg

- have contraindications to carbonic anhydrase inhibitors (eg. severe or absolute glaucoma, adrenocortical insufficiency, hepatic insufficiency, renal insufficiency, sulfa allergy or an electrolyte imbalance such as hyperchloremic acidosis)

- are obese (BMI >30 Kg/m2)

- taking diuretics, blood thinners, or anti-platelet drugs.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Acetazolamide
250 mg, taken orally three times per day
Methazolamide
100mg, taken orally two times per day. A placebo pill will be taken between each dose of methazolamide to match the timing of doses and the number of pills between study arms.
Other:
Placebo
A placebo will be taken three times per day

Locations

Country Name City State
Canada University of British Columbia Kelowna British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Dominelli PB, McNeil CJ, Vermeulen TD, Stuckless TJR, Brown CV, Dominelli GS, Swenson ER, Teppema LJ, Foster GE. Effect of acetazolamide and methazolamide on diaphragm and dorsiflexor fatigue: a randomized controlled trial. J Appl Physiol (1985). 2018 Sep — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Esophageal and Gastric Pressure Baseline, 1, 5, 10, 20, and 30 minutes post loading protocol
Other Heart Rate Baseline, 1, 5, 10, 20, and 30 minutes post loading protocol
Other Beat-by-beat blood pressure Baseline, 1, 5, 10, 20, and 30 minutes post loading protocol
Primary Change in trans-diaphragmatic pressure generation to supramaximal phrenic nerve stimulation following inspiratory threshold loading. Baseline, 1, 5, 10, 20, and 30 minutes following the loading protocol for each arm of the study
Primary Change in plantar flexor muscle group torque generation to supramaximal tibial nerve stimulation following an isometric loading protocol Baseline, 1, 5, 10, 20, and 30 minutes following the loading protocol for each arm of the study
Secondary Maximal inspiratory pressure maneuvers Baseline and immediately following loading protocol
Secondary Maximal Voluntary Contraction of the Plantar Flexor Muscle Group Baseline and immediately following the loading protocol
Secondary Contraction time and half-relaxation time Baseline, 1, 5, 10, 20, and 30 minutes post loading protocol
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