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a clinical study comparing the success rate of pulpotomy using sodium hypochlorite and Cold saline with EDTA as heamostatic and disinfacting agents

“A Comparative Evaluation Of Treatment Outcome Of Two Different Methods Of Full Pulpotomy Using 2.5% Sodium Hypochlorite versus Cryotherapy With Cold saline (2.5° C) Along With 17 % EDTA Solution In Patients With Symptomatic Irreversible Pulpitis - A Randomized Clinical Study. ?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043061
Enrollment
60
Registered
2022-06-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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: Cryo therapy With Cold saline (2.5° C) As Haemorrhage control Along With 17 % EDTA Solution as disinfectant for 5 minutes Control Intervention1: Conventioal Method: Convent

Sponsors

Dr Rohan Jiteshkumar Doshi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Systemically healthy patients (Category: American Society of Anaesthesiologists class 1) (ASA House of Delegates 2014) age between 18-60 years with maxillary or mandibular molar teeth diagnosed with symptomatic irreversible pulpitis will be included. 2. Patient with history of spontaneous/lingering pain/nocturnal pain in relation to maxillary or mandibular molar. 3. A written informed consent will be taken from all the patients and only those patients ready to sign the consent form, willing to participate and come for multiple visit for follow-up will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Non restorable/ badly broken/ necrosed tooth/ tooth with sinus tracts/local gum swelling/ periodontally compromised tooth/ tooth with heavy occlusal forced/ tooth with negative pulp sensibility test/ tooth with any developmental anomalies are excluded from study. 2. Radiographic evidence of peri/inter radicular lesions, internal/external root resorption, pulp stone in pulp chamber and open apex will be excluded from the study 3. Pregnant and lactating patients will be excluded from study.

Design outcomes

Primary

MeasureTime frame
Success of Pulpotomy ProcedureTimepoint: 1.5 Years

Secondary

MeasureTime frame
Tertary Dentin FormationTimepoint: 1.5 years

Countries

India

Contacts

Public ContactDr Rohan Jiteshkumar Doshi

Sumandeep Vidhyapeeth

nshah7873@gmai.com9998994299

Outcome results

None listed

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