Investigating the effect of drain in pain control after laparoscopic cystectomy surgery in women referred to Afzalipur Hospital, Kerma

Not Applicable

Recruiting

Conditions: Ovarian cyst.
N83.29
Other ovarian cysts

Registration Number: IRCT20230130057275N1

Lead Sponsor: Kerman University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 260

Inclusion Criteria

Women aged 18 to 62 without any comorbidities who will undergo laparoscopic ovarian (LOC) for ovarian cysts from January to March 1401 in Afzalipur University Hospital and have no complications during the operation will be studied
Full consciousness
providing informed written consent
not using analgesic before surgery

Exclusion Criteria

History of abdominal and thoracic surgery
psychiatric patients
those with chronic pain in the abdomen, pelvis, systemic disease, fallopian tube abscess (before or during surgery), shoulder pain and trauma
Patients whose laparoscopic surgery is changed to laparotomy
Patients who need a drain due to organ damage, bleeding or infection will be excluded from the study
Patients who develop complications (fever, bleeding, infection at the incision site, atelectasis, subcutaneous emphysema) will also be excluded from the pain intensity study and will be studied only to compare and determine the effect of the drain on the complications

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome of the study is the pain score, which is collected through the VAS questionnaire. Timepoint: VAS pain questionnaire will be measured at 4 hours, 12 hours, 24 hours, 42 hours and 72 hours after surgery. Method of measurement: Visual Analog Scale for Pain (VAS ).

Secondary Outcome Measures

Name	Time	Method
Time to work the bowels. Timepoint: Last hours after surgery. Method of measurement: data collection form through patient declaration.;Days of stay in the hospitalization. Timepoint: hospitalization days after surgery. Method of measurement: Investigation of Medical Record.;Location of pain. Timepoint: 4 hours, 12 hours, 24 hours, 42 hours and 72 hours after surgery. Method of measurement: History and interview with the patient and physical examination.