Ovarian cyst. Other ovarian cysts
Conditions
Interventions
Intervention 1: Intervention group (with drain): Patients will be anesthetized before the start of laparoscopy. The patients will be operated by a surgical team. All patients will be given intravenous
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 62 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNafiseh Seyedi
Kerman University of Medical Sciences
Outcome results
None listed