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Determination of subcutaneous infiltration of ketamine for sedation in patients undergoing TUL surgery under spinal anesthesia in Ahwaz Imam Khomeini hospital in 1397-1398

Determination of subcutaneous infiltration of ketamine for sedation in patients undergoing TUL surgery under spinal anesthesia in Ahwaz Imam Khomeini hospital in 1397-1398

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191227045906N1
Enrollment
60
Registered
2020-05-14
Start date
2020-02-08
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

Urological services with urine virtual stone. Calculus of lower urinary tract

Interventions

Intervention 1: Intervention group: Patients in the intervention group will receive 0.5 mg / kg of subcutaneous ketamine and will receive o2 facial mask therapy with flow = 5lit / min. Intervention 2:

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Spinal anesthesia contraindication TUL surgery candidate ASAI-II class

Exclusion criteria

Exclusion criteria: History of hypertension Hyperthyroidism Psychiatric disorders Allergy to ketamine Kidney or liver failure Intracranial seizures or hypertension Drug or drug abuse within six months Spinal anesthesia contraindication

Design outcomes

Primary

MeasureTime frame
RR. Timepoint: Continuously and every 15 minutes. Method of measurement: It will be continuously measured during the operation and will be recorded and specified every 15 minutes by the capnogram.;HR. Timepoint: Continuously and every 15 minutes. Method of measurement: It will be continuously measured during the operation and will be recorded every 15 minutes by ECG.;BP. Timepoint: Continuously and every 15 minutes. Method of measurement: It will be continuously measured during the operation and will be recorded every 15 minutes by NIBP.;Pain. Timepoint: ?Every 30 min in operation room and one hour and two hours after surgery in recovery. Method of measurement: The amount of pain is measured according to the VAS.;Chill rate. Timepoint: At zero times, 30 minutes, one hour and two hours after the end of surgery and in recovery. Method of measurement: It will be measured based on observation and questioning of the patient and based on crossley division.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKaveh Behaeen

Ahvaz University of Medical Sciences

drbehaeen-k@ajums.ac.ir+98 61 3336 5975

Outcome results

None listed

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