Effect of Aromatherapy with Rose extract in controlling postoperative pai

Phase 2

Recruiting

• Conditions: Condition 1: Pain localized to other parts of lower abdomen. Condition 2: Inguinal hernia.; Pain localized to other parts of lower abdomen; Inguinal hernia

• Registration Number: IRCT201703139597N3
• Lead Sponsor: Vice-chancellor of Research and Technology, Hamadan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

(a)Age of 20-50 years; (b) Patients with class 1 or 2 according to the American Society of Anesthesiology scoring criteria; (c) No history of opium and psychotropic drugs; (d) No Long-term used anti inflammatory non-opoid; (e)No systemic disease; (f)Not sensitive to used drugs ; (g)Woman is not pregnant.
Exclusion criteria: (a) Lack of access to the patient for measuring pain; (b)the patient's inability to determine the pain score for any reason; (c) Morbidity sensitivity to the Rose extraction in the intervention group.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: 1, 6, 12, , and 24 hours after surgery. Method of measurement: Visual Analog Scale (VAS).

Secondary Outcome Measures

Name	Time	Method
Side effects of drugs. Timepoint: 1, 6, 12 and 24 hours after surgery. Method of measurement: questionnaire.;Hemodynamic status. Timepoint: 1, 6, 12 and 24 hours after surgery. Method of measurement: Esphigmomanometery and pulse oximetry.;Analgesic dosage used. Timepoint: 1, 6, 12 and 24 hours after surgery. Method of measurement: questionnaire.