Investigating the effect of pain intensity after mandibular wisdom tooth surgery in patients receiving starch powder and acetaminophen

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20250202064601N1

Enrollment

Registered

2025-03-01

Start date

2024-01-21

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Third Molar teeth surgery.

Interventions

Intervention 1: Intervention group: aricolat powder recievers. Intervention 2: Control group: Acetaminophen recipient group.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Lower wisdom tooth surgery required

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 4 Hours. Method of measurement: Visual Analog Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Mardani

Shiraz University of Medical Sciences

arefeh.nsr79@gmail.com+98 71 3627 0861

Outcome results

None listed

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