JPRN-jRCTs051210028
Recruiting
Phase 2
A double-blind, randomized, controlled trial to evaluate the efficacy of carbon dioxide paste in patients after neck dissection
Hasegawa Takumi0 sites20 target enrollmentMay 24, 2021
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Hasegawa Takumi
- Enrollment
- 20
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients who are 20 years of age or older at informed consent
- •2\.Patients with postoperative scarring pain after unilateral neck dissection
- •3\.Patients from 6 months to 3 years after neck dissection
- •4\.Patients with a VAS score of 1 or more but for neck pain
- •5\.Patients who decide to participate in this clinical study by free will
Exclusion Criteria
- •1\.Patients with drug sensitivity such as allergies
- •2\.Patients with peripheral arterial disease and ischemia (Fontaine III \-IV), Patients with ischemic cerebral artery disease
- •3\.Patients with heart failure and severe ischemic heart disease
- •4\.Female patients who are pregnant, lactating, seeking to become pregnant within the study period, or who are unable to accept contraception
- •5\.Patients with severe respiratory disease with SpO2: 90% or less
- •6\.Patients who have difficulty applying the paste, such as those with skin ulcers or skin diseases larger than 4cm x 4cm x 1cm
- •7\.Patients who are deemed inappropriate by the investigators of this clinical study.
Outcomes
Primary Outcomes
Not specified
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