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Effect of root canal preparation under continuous irrigation on postoperative pain in teeth with symptomatic apical periodontitis: a preliminary randomized controlled prospective clinical trial

Effect of root canal preparation under continuous irrigation on postoperative pain in teeth with symptomatic apical periodontitis: a preliminary randomized controlled prospective clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190725006
Enrollment
Unknown
Registered
2019-07-25
Start date
2018-03-13
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

Fifty patients having symptomatic apical periodontitis with a preoperative and percussion pain of visual analog scale (VAS) more than 50 were included in this study apical periodontitis&#44

Interventions

Conventional preparation and irrigation were performed in this group. 2 mL 2.5% NaOCl was used between each pecking motion. ,In this group&#44
root canal preparation was performed under continuous irrigation with saline solution at room temperature. Surgical motor (Implantmed
W&H&#44
Bürmoos&#44
Austria) was integrated to the endodontic motor.
Experimental Procedure/Surgery,Experimental Procedure/Surgery
Conventional preparation (Control group),Preparation under continuous irrigation

Sponsors

No sponsor
Lead Sponsor
No sponsor
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Criteria for inclusion were limited to patients having symptomatic apical periodontitis (for both pre-operative and percussion pain) with a Visual Analog Scale (VAS) of more than 50 related with mandibular or maxillary molar tooth, patients having molar tooth having periapical lesion score 1 or 2 according to the scoring system described by Ørstavik et al. (Ørstavik et al. 1986), and patients aged 18-65 years.

Exclusion criteria

Exclusion criteria: Exclusion criteria include patients having systemic diseases or allergic reactions, patients having psychiatric disorders, patients under analgesics medication at within 24 hours prior to root canal treatment or antibiotic medication at least one week before the appointment, presence of a swelling, sinus tract, severe periodontal disease or a periodontal pocket more than 3 mm, previous root canal treatment and patients with tooth associated with root resorption, root fracture or ankylosis.

Design outcomes

Primary

MeasureTime frame
Pain 1 week VAS

Secondary

MeasureTime frame
Postoperative percussion pain 1 week VAS

Countries

Turkey

Contacts

Public ContactHakan Arslan

Ataturk University

dt_hakan82@hotmail.com05339351238

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026