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The effect of oral Clonidine and Tranexamic on blood loss during surgery

Comparison the effect of oral Clonidine and Tranexamic acid before Surgery on blood loss in lumbar spine surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110528006617N4
Enrollment
90
Registered
2020-07-11
Start date
2019-09-23
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

General anesthesia. Intervertebral disc disorders with myelopathy, lumbar region

Interventions

Intervention 1: Intervention group: The first intervention group(Tranexamic acid) receive 600mg oral Tranexamic acid and one placebo tablet 2 hour before surgery. Induction of anesthesia with 0/05mg/k

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age between 20 – 65 year patients who consent to the informed consent to participate in the study ASA class 1 ,2

Exclusion criteria

Exclusion criteria: Beta blocker and Calcium blocker usage sedative drugs usage Opioids usage addiction to Alcohol allergic reaction to drugs allergic reaction to Local anesthetic drugs history of lumbar surgery risk factor of thrombosis anticoagulants drugs usage Digoxin usage Aspirin uage

Design outcomes

Primary

MeasureTime frame
Systolic Blood Pressure. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: mmHg , SAADAT Sphygmomanometer monitoring.;Diastolic Blood Pressure. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: mmHg , SAADAT Sphygmomanometer monitoring.;Mean Artherial Pressure. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: mmHg , SAADAT Sphygmomanometer monitoring.;Heart rate. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: beat/min , SAADAT ECG monitoring.;Volume Of Blood Loss. Timepoint: enter to the recovery, export from recovery. Method of measurement: Milliliter,volume of blood in the suction, Bloody gas.;Surgeon Satisfaction. Timepoint: End of the surgery. Method of measurement: Likert Scale.

Secondary

MeasureTime frame
Hypotension. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: mmHg, SAADAT Sphygmomanometer monitor.;Hypertension. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: mmHg, SAADAT Sphygmomanometer monitor.;Tachycardia. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: beat/min ,SAADAT ECG monitoring.;Bradycardia. Timepoint: Basic time(two hours before surgery), before anesthesia induction, 1,3,5,10,15 min after anesthesia, every 15 min during surgery, in the time of patient enter to the recovery. Method of measurement: beat/min ,SAADAT ECG monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Masoudifar

Esfahan University of Medical Sciences

Masoudifar@med.mui.ac.ir+98 31 3620 2020

Outcome results

None listed

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