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Static navigation in endodontic microsurgery

Investigating static navigation on the accuracy and efficiency of the endodontic microsurgery: A pilot study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250110064333N1
Enrollment
10
Registered
2025-03-27
Start date
2025-04-21
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Chronic Apical periodontitis. Chronic apical periodontitis

Interventions

Intervention 1: Intervention group: endodontic surgery with static navigation (3D guide designed specifically for each patient via combination of data from CBCT and intraoral scan). Intervention 2: Co

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor
Dental Research Center of MUMS
Collaborator
Dental Materials Research Center of MUMS
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: age range between 18 to 65 years the periapical lesion associated with only one tooth a tooth needing endodontic microsurgery in mandibular posterior region cortical plate thickness between 2 to 5 millimeters in CBCT image

Exclusion criteria

Exclusion criteria: Incompatibility and instability of the designed guide with the surgical site after flap elevation Patients who cannot tolerate the designed guide during surgery Patients who do not return for the second CBCT image Patients who are unavailable on days 1, 3, and 7 after surgery

Design outcomes

Primary

MeasureTime frame
Accuracy of osteotomy. Timepoint: post surgery. Method of measurement: superimposition of pre and post operative CBCTs.;Duration of osteotomy and apicoectomy. Timepoint: during the osteotomy and apicoectomy phases of the surgery. Method of measurement: separately recording the time from the beginning to the end of the osteotomy and paicoectomy phases.;Number of intraoperative errors. Timepoint: intraoperative. Method of measurement: recording possible errors during surgery.;Postoperative pain. Timepoint: days 1, 3 and 7 after surgery. Method of measurement: visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Karimpour

Mashhad University of Medical Sciences

samasamafara@gmail.com+98 51 3882 9501

Outcome results

None listed

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