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Effective comparision of Apotel versus Morphine in reducing of post pure head trauma headache

Effective comparision of Apotel versus Morphine in reducing of post pure head trauma headache

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204127327N2
Enrollment
60
Registered
2012-05-26
Start date
2012-05-04
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

Traumatic headache. Chronic post-traumatic headache

Interventions

Intervention 1: In intervention group, 1 gr Apotel will be diluted in 100 cc normal saline and be infused in 10 minutes. Intervention 2: In control group, 0.1mg/kg Morphine will be infused.
Treatment - Drugs
In intervention group, 1 gr Apotel will be diluted in 100 cc normal saline and be infused in 10 minutes
In control group, 0.1mg/kg Morphine will be infused

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All patients with head trauma will be enrolled after obtaining the neourosurgery service examination result that there is no pathologic findings. Patients who have GCS14 or less or are older than 65 or age under 18 years old are excluded

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache. Timepoint: one week. Method of measurement: Numeric pain scale.

Secondary

MeasureTime frame
Hypotension. Timepoint: 10min. Method of measurement: Barometer.;Hypoxemia. Timepoint: 10 min. Method of measurement: puls oximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Samad shams Vahdati

Tabriz University of Medical Sciences

shams@tbzmed.ac.ir+98 41 1335 2078

Outcome results

None listed

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