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aparoskooppisen paksusuoliresektion leikkauksen jälkeisten kivunhoitomenetelmien vertailu nykytiedon valossa

Phase 1
Conditions
Tutkittavat tulevat paksusuoliresektiotoimenpiteeseen joko paksusuolisyövän tai divertikuloosin vuoksi. Tutkimuksessa selvitetään puudutusmenetelmän vaikutusta toimenpiteen jälkeiseen kivunhoitoon.
MedDRA version: 20.0Level: LLTClassification code 10002183Term: Analgesia intra/post opSystem Organ Class: 100000004865
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
Registration Number
EUCTR2021-000728-36-FI
Lead Sponsor
Tampere University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
255
Inclusion Criteria

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 155
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 100

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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