Comparison effect of ketamine-propofol versus fentanil-propofol for creating analgesia and sedation during limited surgery

Comparison effect of intra-venous ketamine-propofol versus fentanil-propofol for creating analgesia and sedation during limited surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015082522734N2

Enrollment

110

Registered

2015-10-11

Start date

2014-03-21

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Musclu-skeletal trauma. Disorder of bone density and structure, unspecified

Interventions

Intervention 1: Intervention group 1: fentanil 1µg/kg + propofol 1 mg/kg. Intervention 2: Intervention group 2: ketamine 1 mg/kg + propofol 1 mg/kg.

Treatment - Drugs

Intervention group 1: fentanil 1µg/kg + propofol 1 mg/kg

Intervention group 2: ketamine 1 mg/kg + propofol 1 mg/kg

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 18 to 70 y/o; Class ASA I-II Exclusion criteria: Opium users, Sympatomimetics drug users; History of allergy and drug reaction; BMI more than 30 kg/m2

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain relief. Timepoint: 30 minute. Method of measurement: questionnare.	—

Secondary

Measure	Time frame
Vital signs. Timepoint: 30 minute. Method of measurement: questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMani Mofidi

Iran Unuversity of Medical Sciences

mofidi.m@iums.ac.ir; manimofidi@yahoo.com+98 21 6435 2221

Outcome results

None listed

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