NCT07057388

Brief Summary

The study involves two groups in which root canal obturation will be performed using different obturation techniques. Group one consists of participants with the single cone cold lateral condensation method, while group two consists of participants with the continuous wave compaction technique. Postoperative pain will be assessed and compared between the two groups.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 20, 2025

Completed
19 days until next milestone

First Posted

Study publicly available on registry

July 9, 2025

Completed
21 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 30, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2025

Completed
Last Updated

September 11, 2025

Status Verified

January 1, 2025

Enrollment Period

7 months

First QC Date

June 20, 2025

Last Update Submit

September 9, 2025

Conditions

Root Canal Obturation

Outcome Measures

Primary Outcomes (1)

  • comparison of post operative pain

    post operative pain using VISUAL ANALOGUE SCALE (VAS) , two methods of obturation to assess pain after root canal using cold lateral versus heated gutta percha Pre operative pain will be measured on each patient according to visual analogue scale as baseline before intiating the procedure .

    24 hours , 48 hours and 1week

Study Arms (2)

Group one receiving cold lateral condensation obturation

NO INTERVENTION

conventional method of obturation is used

Group 2 receiving obturation through continous wave compaction

EXPERIMENTAL

heated gutta percha using continous wave compaction

Device: continous wave compaction

Interventions

continous wave compactionDEVICE

post operative pain measurement using continous wave compaction

Group 2 receiving obturation through continous wave compaction

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • irreversible pulpitis

You may not qualify if:

  • periapical abcess

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

28 Military Dental Centre

Lahore, Punjab Province, Pakistan

Location

Study Officials

  • Imran Khan, BDS FCPS

    28 military dental centre

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
post graduate resident

Study Record Dates

First Submitted

June 20, 2025

First Posted

July 9, 2025

Study Start

January 1, 2025

Primary Completion

July 30, 2025

Study Completion

August 30, 2025

Last Updated

September 11, 2025

Record last verified: 2025-01

Locations

PA(1)