Postoperative Pain. Acute Pain
Conditions
Interventions
Intervention 1: In intervention group patients received infrared and red laser(PLP-IR-808nm-200mw, PLP-R-650nm-100mw) radiation manufactured by COL center-Canada once after the end of surgery. Interve
Prevention
In intervention group patients received infrared and red laser(PLP-IR-808nm-200mw, PLP-R-650nm-100mw) radiation manufactured by COL center-Canada once after the end of surgery
In control group patients received off laser once after the end of surgery
Sponsors
Ahvaz Jundishapur University of Medical Sciences, Vice Chancellor for Research and Technology
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria : Pregnant women 18-40 years ; gravid 1,2 ; ASA Class I,II Exclusion Criteria : patient refusal ; elevated intracranial pressure ; bleeding diathesis ; infection at the site of planned needle puncture ; lower extremity peripheral neuropathy ; classic cesarean scar ; malignancy ; benign tumors with probability of being malignant ; hypersensitivity to light like lupus ; history of convulsion
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 1,4,8,12,16,24 hours after end of anesthesia. Method of measurement: VAS questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Opioid Consumption. Timepoint: 24 hours after surgery. Method of measurement: questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Sholeh Nesioonpour
School of Medicine , Ahvaz Jundishapur University of Medical Sciences
Outcome results
None listed