post operative pain control

Long-acting local anesthetic infiltration in surgical wound for post operative pain control in zygomatico maxillary complex fracture

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT201406201772N14

Enrollment

Registered

2014-06-27

Start date

2014-05-22

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

post operative pain control. local Anesthetic

Interventions

Intervention 1: Surgical site infiltrated before wound closure with 10 ml Bupivacaine 0.5%. Intervention 2: Surgical site infiltrated before wound closure with placebo.

Treatment - Drugs

Surgical site infiltrated before wound closure with 10 ml Bupivacaine 0.5%

Surgical site infiltrated before wound closure with placebo

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion: age from 20 to 60 people who are going to have open reduction for Zygomatic fracture Exclusion criteria : Addiction, Seizure, psychopathic conditions and refuse to participate.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 0, 2, 4, 6, 12 and 24 hours after operation. Method of measurement: Visual Analogue Scale.	—

Secondary

Measure	Time frame
Opioid cosumption. Timepoint: 0, 2, 4, 6, 12 and 24 hours after operation. Method of measurement: Total Dose.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDawood Aghamohammadi

Tabriz university of medical science/fuculty of medicin/ Anesthesiology Dept

aghamohammadid@tbzmed.ac.ir+98 41 1381 8940

Outcome results

None listed

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