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A study comparing cold Comparison of cooling treatment and laser in controlling bleeding and reducing pain after pulpotomy in adults with painful permanent teeth.

Comparative evaluation of effect of Cryotherapy and Laser application on haemostasis and postoperative pain in Total Pulpotomy procedure in mature permanent teeth with symptomatic irreversible pulpitis - A Randomized Controlled Trial. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113916
Enrollment
36
Registered
2026-07-14
Start date
Unknown
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

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: Cryotherapy: Mature permanent teeth with symptomatic irreversible pulpitis undergoing Total Pulpotomy using Cryotherapy. The pulp chamber will be continuously lavaged with 2 to 4 degre

Sponsors

Dr Anjali Ashokkumar Ahuja
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Teeth diagnosed with symptomatic Irreversible Pulpitis. 2. Patients aged between 18 to 60 years. 3. Mandibular first and second molars with complete root development, no periodontal problems. 4. Teeth with deep caries detected on periapical radiography. 5. Teeth having vital pulp and responded to the cold test.

Exclusion criteria

Exclusion criteria: Patients who are medically compromised. Patients who had taken antibiotics in last 1 month Patients who had used nonsteroidal anti-inflammatory drugs within the last twelve hours. Pregnant and lactating women. Teeth that could not be restored or required a post and core. Teeth that had non vital pulp, did not respond to the cold test. Teeth that had no exposed pulp after nonselective caries removal. Teeth with periodontal pocket larger than 3 mm. Teeth that have been previously accessed. Teeth associated with periapical lesion visible on radiograph.

Design outcomes

Primary

MeasureTime frame
Time taken to achieve haemostasisTimepoint: At Baseline

Secondary

MeasureTime frame
Postoperative pain using VAS scaleTimepoint: Every 24 hours for 7 days

Countries

India

Contacts

Public ContactDr Sulabha Radke

Government Dental College and Hospital, Nagpur

sulabharadke@gmail.com9823262628

Outcome results

None listed

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