UnknownNot Applicable

Patients' Quality of Life After Pilonidal Cyst Operations.

Lithuania100 participantsStarted 2020-09-01

Plain-language summary

Biomedical research consists of two main parts. In the first part, the pilonidal cyst-specific quality of life questionnaire is compiled, adapted, validated, tested for suitability in assessing patients after pilonidal cyst operations. The second part will compare two pilonidal cyst operations. A prospective, comparative, randomized clinical study will be conducted.

Who can participate

Age range18 Years – 75 Years

SexALL

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Inclusion criteria

✓. Patients aged 18-75 (men and women)
✓. Chronic symptomatic (primary or recurrent) pilonidal cyst
✓. American Society of Anesthesiologists physical status I to III
✓. Signed the person's information and consent form to participate in the study.

Exclusion criteria

✕. Acute pilonidal cyst
✕. Patients who do not speak Lithuanian
✕. Cognitive, visual, auditory and locomotor system disorders
✕. Insufficiency of kidneys, liver, cardiopulmonary system
✕. Refuses to participate in the study

What they're measuring

Pain after surgery

Timeframe: One week after surgery

Trial details

NCT IDNCT05982028

SponsorLithuanian University of Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-09-01

View on ClinicalTrials.gov More Pilonidal Cyst trials