Stress level after surgery in spinal anesthesia

Post traumatic stress and awareness in traumatic lower limb surgery patients after neuraxial anesthesia : A randomized clinical trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190819044559N3

Enrollment

220

Registered

2020-06-13

Start date

2019-08-29

Completion date

Unknown

Last updated

2020-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-traumatic stress. Post-traumatic stress disorder, acute

Interventions

Intervention 1: Intervention group: Propofol infusion of 25-75 micro grams per kilogram per minute is recommended. Intervention 2: Control group: 1-2 mg of midazolam PRN is recommended.

Eligibility

Sex/Gender

All

Age

18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Trauma and candidate for lower extremity surgery Age between 18-50 years

Exclusion criteria

Exclusion criteria: History of psychiatric disorders Previous history of lower leg surgery Refusal to attend the study More than 3 hours of surgery duration Severe blood loss Decrease in consciousness and endotracheal intubation during surgery

Design outcomes

Primary

Measure	Time frame
??Stress level after trauma according to Mississippi questionnaire. Timepoint: One day before surgery, after transfer to Recovery,1 and 7 days after surgery. Method of measurement: Mississippi questionnaire.;Awareness level after neuraxial anesthesia with midazolam or propofol. Timepoint: One day before surgery, after transfer to Recovery,1 and 7 days after surgery. Method of measurement: The Brace questionnaire.	—

Measure

Time frame

??Stress level after trauma according to Mississippi questionnaire. Timepoint: One day before surgery, after transfer to Recovery,1 and 7 days after surgery. Method of measurement: Mississippi questionnaire.;Awareness level after neuraxial anesthesia with midazolam or propofol. Timepoint: One day before surgery, after transfer to Recovery,1 and 7 days after surgery. Method of measurement: The Brace questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMorteza Hashemian

Kerman University of Medical Sciences

mortezahashemian@kmu.ac.ir+98 34 3223 5011

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026