Study to compare the amount of bleeding with or without discontinuing blood thinners in patients who required teeth extraction.

A comparative study to assess bleeding with or without discontinuing antiplatelet therapy in patients undergoing dental extraction.

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/03/032465

Enrollment

Registered

2021-03-31

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: I999- Unspecified disorder of circulatory system

Interventions

Intervention1: Individuals undergoing anti-platelet therapy who report to Department of Oral and Maxillofacial Surgery on daily OPD basis requiring extraction will be a part of the study.: Antiplatele

Eligibility

Inclusion criteria

Inclusion criteria: . Patients on antiplatelet therapy requiring extraction. 2. Patients requiring single or multiple [up to 3] extractions. 3. Patients willing to participate in the study. 4. Patients on antiplatelet therapy for preventive prophylaxis.

Exclusion criteria

Exclusion criteria: . Patients with hematological, renal, or liver disease. 2. Patients with bone marrow disorders or alcoholism. 3. Patients on any concurrent medication affecting hemostasis such as oral or parental anticoagulants. 4. Patient on antiplatelet therapy as secondary prophylaxis 5. Pregnant and lactating women. 6. Patient with medical history which is an absolute contraindication for extraction.

Design outcomes

Primary

Measure	Time frame
Intraoperative bleedingTimepoint: 30 minutes , 1 hour	—

Secondary

Measure	Time frame
Postoperative duration of bleedingTimepoint: 24 hours	—

Countries

India

Contacts

Public ContactDrDimple k Chandra

HOD

sanjoshi99@gmail.com9869057337

Outcome results

None listed

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