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The effect of low-dose intravenous ketamine on shoulder pain

The effect of low-dose intravenous ketamine on shoulder pain following caesarean section under spinal anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016041627242N2
Enrollment
80
Registered
2016-07-06
Start date
2016-04-18
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

The effect of ketamin on shoulder pain. Other and unspecified general anaesthetics

Interventions

Intervention 1: All the patients in the intervention group receive 500-1000 cc of ringer before performing spinal anesthesia.Before spinal anesthesia standard monitoring including blood pressure(systo
Treatment - Drugs
Treatment - Other
All the patients in the intervention group receive 500-1000 cc of ringer before performing spinal anesthesia.Before spinal anesthesia standard monitoring including blood pressure(systolic and diastoli
All the patients in control group receive 500-1000 cc of ringer before performing spinal anesthesia.Before spinal anesthesia standard monitoring including blood pressure(systolic and diastolic),heart

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: pregnant women wich age is between 15-40 ywers old, and will be c/s under spinal anastesia Exclusion criteria: Interdict scientific forbide(rise ICP; eklampsy; pereklampsy; head truma; primery hypertension; brain tumor;cerebrovascular accsident in past); addiction; sensivity to ketamine; cronic shulder pain; history of psychiatric disease; pregnancy hypertension; history of fracture;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Shoulder pain. Timepoint: After intervention in first 24 hour. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Hallucination. Timepoint: After interventin in first 3 hour. Method of measurement: Taking history.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSolmaz dastras

Sabzevar University of Medical Sciences

Solmazdastras@yahoo.com+98 51 4421 7383

Outcome results

None listed

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