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the survey of comparative of Clonidine and conventional methods on post operative analgesia

Comparative of Clonidine and conventional methods on post operative analgesia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012091310340N6
Enrollment
44
Registered
2012-10-04
Start date
2011-04-14
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

herniotomy. Diseases of mediastinum, not elsewhere classified

Interventions

Intervention 1: group 2: 0.5 mg / kg pethidine. Intervention 2: Group 1:clonidine 4 micrograms per kilogram.
Treatment - Drugs
group 2: 0.5 mg / kg pethidine
Group 1:clonidine 4 micrograms per kilogram

Sponsors

Golestan university of mecdical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 3 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: herniotomy surgery; 1 to 3 years-old. Exclusion criteria: pain before surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: FLACC SCALE. Method of measurement: After surgery.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactdoctor Abdolrahmane Tofighi Rad

Golestan university of medical sciences

kazemnejad1341@yahoo.com+98 17 1442 1651

Outcome results

None listed

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