NCT Number: NCT00233844
Studying the Analgesic Mechanism of the "Cough-trick"
The aim of the trial is to study the possible mechanism of the pain reducing effect of CT at peripheral venipuncture
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Notify MeKey information
Conditions
Age range
20 year–35 year
Sex eligibility
Male
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Male volunteers aged 20-40 years, height 165-190 cm.
- Physical status I according to American Society of Anesthesiologists (ASA) classification.
- Straight run of the vein on the dorsum of the non-dominant hand at least 4 cm long and 3 mm thick
- No analgesics, anticoagulants and/or antiplatelet agents, sedatives or alcohol
Exclusion criteria
- History of peripheral neuropathy
- Abnormal skin conditions (infection, scars, psoriasis, eczema)
- Unsuccessful venipuncture
- Inflamed site of VP within 1 week after VP
Treatment and study plan
Primary outcomes
-
Pain intensity measured on 100 mm Visual Analogue Scale scale (VAS-100) where 0 = no pain and 100 = maximal pain
Time frame: immediately during venipuncture
Secondary outcomes
-
Heart rate, beats per minute
Time frame: 5 min during venipuncture
Sponsors and collaborators
Lead sponsor
University Medicine Greifswald
Other
Registry information
Official study title
Studying the Analgesic Mechanism of the "Cough-trick" - Randomized Crossover Volunteer Study
Important dates
- Study start
- 2004
- Primary completion
- 2008
- Study completion
- 2008
- First posted
- Oct 6, 2005
- Registry last updated
- Jun 11, 2026
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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