Skip to content

Comparative evaluation of cleaning efficacy of "5.25% Sodium Hypochlorite gel" and "5.25% Sodium Hypochlorite solution" in multi-rooted teeth with infection.

Comparative evaluation of antimicrobial efficacy of 5.25% Sodium Hypochlorite gel And 5.25% Sodium Hypochlorite solution as a root canal disinfectant in multi-rooted teeth with primary endodontic lesion â?? A Randomized Clinical Study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040647
Enrollment
42
Registered
2022-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

None listed

Interventions

Intervention1: 5.25% sodium hypochlorite gel: 5.25% sodium hypochlorite gel for root canal disinfection for 5 minutes during chemomechanical preparation of the root canals during the first visit(sitti

Sponsors

Niral Kotecha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Systemically healthy patients, i.e., Class I patients according to American Society of Anaesthesiology [ASA] classification having multirooted teeth diagnosed with pulpal necrosis with asymptomatic apical periodontitis will be included. 3. Teeth with at least three intact coronal walls indicated for endodontic therapy will be included. 4. A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Teeth with symptomatic reversible or irreversible pulpitis, acute apical abscess, phoenix abscess, weeping canals, periapical cyst, vertical root /crown fracture, root caries, root resorption, calcified canals, severe dilacerations will be excluded. 2. Teeth with developmental anomaly or congenital defects will be excluded. 3. Patients on antibiotic therapy will be excluded from the study. 4. Pregnant and lactating women will be excluded.

Design outcomes

Primary

MeasureTime frame
Viable organisms will be counted as Colony Forming Units (CFU) per mlTimepoint: after 48 hrs of intervention and incubation of sample

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactNiral Kotecha

K.M.Shah Dental College and Hospital

kotechaniral@gmail.com8861603166

Outcome results

None listed

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