efficiency of amoxicillin in 7days to decrease the rate of the complication from inflammation and infection after 3rd mandibular molar surgery

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20160809002

Enrollment

Registered

2016-08-09

Start date

2016-08-15

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

post&#45

Interventions

prophylaxis,non prophylax

use amoxicillin 500mg 1*3 7days paracetamol 500mg 1*prn 15 tabs ibuprofen 400mg 1*3 15 tabs,use paracetamol 500mg 1*prn 15 tabs ibuprofen 400mg 1*3 15 tabs

Experimental Drug,Experimental Drug

Eligibility

Sex/Gender

All

Age

15 Years to 60 Years

Inclusion criteria

Inclusion criteria: 3rd mandibular impacted pateints in dental depart. phayao hospital

Exclusion criteria

Exclusion criteria: low immune suprainfection amoxicillin allergy

Design outcomes

Primary

Measure	Time frame
sign of inflammation and infection 7 days post-op surgery observation	—

Secondary

Measure	Time frame
post-op complication 7 days post-op surgery observation	—

Countries

thailand

Contacts

Public Contactnattha chumsuphanwaree

phayao hospital

dentphayao_hp@hotmail.com0814730068

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026