Clinical Trials Logo
  1. Home
  2. Healthy Subjects
  3. NCT01102634
  4. Details
NCT01102634 Clinical Trial

Effects of Acu-Transcutaneous Electrical Nerve Stimulation (Acu-TENS) on Post-exercise Blood Lactate and Excessive Post-exercise Oxygen Consumption (EPOC)

Healthy Subjects Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01102634
Other study ID # HSEARS20100407006
Secondary ID
Status Recruiting
Phase N/A
First received April 8, 2010
Last updated April 12, 2010
Start date April 2010

Study information
Verified date April 2010
Source The Hong Kong Polytechnic University
Contact Alice Jones, PhD, FACP
Phone (852) 27666749
Email alice.jones@polyu.edu.hk
Is FDA regulated No
Health authority Hong Kong: Ethics Committee
Study type Interventional

Clinical Trial Summary

The study aims to investigate the effect of Acu-TENS on post-exercise blood lactate level and EPOC

Recruitment information / eligibility
Status Recruiting
Enrollment 20
Est. completion date
Est. primary completion date August 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

- with normal health (no known history of cardiovascular, pulmonary, metabolic or musculoskeletal diseases)

Exclusion Criteria:

- unable to communicate and follow the exercise procedures

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Device:
• Transcutaneous electrical nerve stimulation (TENS)
Application of TENS over acupuncture points
• Transcutaneous electrical nerve stimulation (TENS)
Placebo

Locations
Country Name City State
China Cardiopulmonary and Exercise Physiology Laboratory, The Hong Kong Polytechnic University Hong Kong Hong Kong

Sponsors (1)
Lead Sponsor Collaborator
The Hong Kong Polytechnic University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Blood lactate level Finger pick method - measured by Lactate Plus (Nova Biomedical, USA) Before exercise No
Primary Blood lactate level Finger pick method - measured by Lactate Plus (Nova Biomedical, USA) Immediately post exercise No
Primary Blood lactate level Finger pick method - measured by Lactate Plus (Nova Biomedical, USA) 15 minutes post exercise No
Primary Oxygen consumption measured by K4b2 (Cosmed, Italy) Measurements continued during exercise and until heart rate returned to baseline No
Secondary Heart rate measured by Polar heart rate monitor (RS800CX, Polar Electro, Finland) Measurements continued during exercise and until heart rate returned to baseline No
See also
  Status Clinical Trial Phase
Completed NCT05483998 - A Study to Evaluate Single and Multiple Doses of TLC-2716 in Healthy Participants Phase 1
Recruiting NCT02235012 - Cognitive Biases Under Ketamine N/A
Recruiting NCT02417714 - Prospective Evaluation of Next Generation CT Reconstruction (NextGenIR)
Completed NCT04418973 - Analysis of Breath Volatile Organic Compounds After Dyspnea Induced in the Healthy Subject. N/A
Completed NCT05088343 - Effect of Hetrombopag on the Pharmacokinetics of Rosuvastatin in Healthy Subjects Phase 1
Not yet recruiting NCT06248801 - Vildagliptin and Metformin Tablets 50/1000 mg Relative to GALVUS MET (50mg/1000 mg) Tablets Phase 1
Terminated NCT04068259 - Single Ascending Dose Study of PBI-4547 in Healthy Subjects Phase 1
Completed NCT03279302 - Trial to Evaluate the PK Profile of Glepaglutide (ZP1848) After a Single IV and After Multiple SC Injections in Healthy Subjects Phase 1
Not yet recruiting NCT06233162 - Febuxostat 80 mg Tablets Relative to Feburic® 80 mg Tablets Phase 1
Recruiting NCT04159844 - Evaluation of the Stiffness and Pressure Applied on the Lower Leg by a New Compression Bandage on Healthy Subjects N/A
Completed NCT06137911 - Evaluation of Safety, Tolerability & Pharmacokinetics of JYP0061 in Healthy Adults. Phase 1
Completed NCT04849286 - Measurement of HTL0016878 in Cerebrospinal Fluid Phase 1
Not yet recruiting NCT06233227 - Dutasteride Soft Capsule 0.5 mg Relative to Avodart 0.5 mg Soft Capsule Phase 1
Completed NCT04096157 - A Study to Assess Isavuconazole Following a Single Dose of Isavuconazonium Sulfate Intravenous Solution Via Nasogastric (NG) Tube Compared to a Single Dose of Oral Capsules Under Fasting Conditions in Healthy Participants Phase 1
Completed NCT01200368 - Trial Evaluating a 13-valent Pneumococcal Conjugate Vaccine Given With Diphtheria, Tetanus, and Acellular Pertussis Vaccine (DTaP) in Healthy Japanese Infants Phase 3
Recruiting NCT05805033 - Peri-Implant Soft Tissue Integration in Humans: Influence of Material N/A
Completed NCT04027803 - Comparative Study of Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of Single Intravenous Doses of BCD-148 and Soliris® Phase 1
Recruiting NCT03467880 - Multicenter Study of Impulse Oscillometry in Chinese N/A
Completed NCT02903095 - Single Ascending Dose Study of TD-1439 in Healthy Subjects Phase 1
Active, not recruiting NCT02341508 - A Phase 1a, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate Lpathomab in Healthy Volunteers Phase 1