Evaluation of the preventive effects of Aminophylline Plasil and Paracetamol on the pain intensity after strabismus surgery

Evaluation of the preventive effects of Aminophylline, Plasil and Paracetamol on the pain intensity after strabismus surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20150106020588N6

Enrollment

120

Registered

2019-07-28

Start date

2017-05-07

Completion date

Unknown

Last updated

2019-10-07

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

Conditions

strabismus. Exotropia

Interventions

Intervention 1: Control group: no intervention. Intervention 2: Intervention group: 0.1 mg per kg Metoclopiramide slow IV 15 mins befor surgery ends. Intervention 3: Intervention group: 3mg per kg Ami

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: abbsence of taking analgesics, paracetamol, aminophylline or plasil in 24 hours before the surgery Filled written informed consent

Exclusion criteria

Exclusion criteria: Any background of allergy to Aminophylline Plasil and Paracetamol Reporting chronic pain prolonged more than 6 months

Design outcomes

Primary

Measure	Time frame
Intensity of pain after strabismus surgery. Timepoint: entering the recovery, 30 , 60 mins and 2 , 4,8,16,24 hours after entering to recovery. Method of measurement: VAS.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDarioush Moradi Farsani

Esfahan University of Medical Sciences

dmoradi@med.mui.ac.ir+98 31 3625 5555

Outcome results

None listed

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