Study the effect of memantine on acute pai

Not Applicable

Recruiting

• Conditions: Condition 1: pain. Condition 2: Hysterectomy.; Acute pain; Acquired absence of genital organ(s)

• Registration Number: IRCT2017070434888N1
• Lead Sponsor: Vice chancellor for research of university of medical sciences of zahedan

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: Female
• Target Recruitment: 60

Inclusion Criteria

Main criteria for entering the study: patient satisfaction, ages 20 to 70, selective hysterectomy surgery.
Main exclusion criteria for the study of liver-renal or cardiac diseases and psychiatric illness that may disturb the patient's assessment, drug addiction or any other psychoactive substance, patient's death, and patient's lack of cooperation

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: At recovery and hours 6, 12, 24, 36 and 48 after surgery. Method of measurement: Score measured by VAS criteria.

Secondary Outcome Measures

Name	Time	Method
Relaxation. Timepoint: At recovery and hours 6, 12, 24, 36 and 48 after surgery. Method of measurement: Relaxation based on Ramsey's relaxation score.;Drug use Required Patient. Timepoint: Within 48 hours after surgery. Method of measurement: Drug use included in patient file.;Complications (nausea and vomiting). Timepoint: Within 48 hours after surgery. Method of measurement: Ask the patient for the presence or absence of nausea and vomiting.