Evaluation of topical ketorolac in minimizing the postoperative sequela associated with removal of the impacted lower wisdom teeth: A randomized clinical study

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

TCTR

Registry ID

TCTR20260301005

Enrollment

Registered

2026-03-01

Start date

2025-12-01

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

pain pain after surgical extraction of lower wisdom teeth

Interventions

drug after extraction,no drug after extraction

Experimental Drug,No Intervention No treatment

drug,control

Eligibility

Sex/Gender

All

Age

18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1- healthy patient. 2- no pregnancy 3- no lactation and no allergy 4- class 1 and 2 of impaction of molar teeth

Exclusion criteria

Exclusion criteria: 1- medically compromised patients 2- allergy for drug 3- pregnancy and lactation 4- class 3 of impaction of third molar

Design outcomes

Primary

Measure	Time frame
pain ONE WEEK Visual analog scale ,TRISMUS one week mouth opening	—

Secondary

Measure	Time frame
healing one week healing score	—

Countries

Iraq

Contacts

Public Contacttabarak waheed

alqadisiyai

Tabarak.Waheed2508m@codental.uobaghdad.edu.iq07870372975

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026