Influence of Sling suture on post-operation complications after extraction of mandibular third molars

Comparison of Sling and Single interrupted suture on post-operation complications after extraction of impacted mandibular third molars

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017100436551N1

Enrollment

Registered

2017-11-11

Start date

2017-10-12

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Condition 1: complication of third molar surgery. Condition 2: gingival recession. Condition 3: periodontal condition. Condition 4: Dehiscence. Condition 5: pain. complication of surgical and medical care, unspecified Gingival recession (generalized)(localized)(postinfective)(post-operative) Other periodontal diseases Disruption of operation wound, not elsewhere classified Other specified disorders of teeth and supporting structures

Interventions

Intervention 1: single interrupted suture: is used to approximate the buccal and lingual flaps. The needle penetrates the outer surface of the first flap.The under surface of the opposite flap is enga

Treatment - Surgery

single interrupted suture: is used to approximate the buccal and lingual flaps. The needle penetrates the outer surface of the first flap.The under surface of the opposite flap is engaged, and, the s

Sling suture:The needle engages the outer surface of the flap and,encircles the tooth. The outer surface of the same flap of the adjacent inter dental area is engaged.The suture is returned to the ini

Eligibility

Sex/Gender

All

Age

18 Years to 25 Years

Inclusion criteria

Inclusion criteria: inclusion criteria:patients who have mandibular third molars with bilaterally identical level of impaction. age 1825 years; smokers; patients with systemic disease; pregnancy or lactation period;use medication in the last 6 months;any inflammation such as acute pericoronitis and periodontal disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: baseline, 2nd, 7th & 14th. Method of measurement: Visual Analogue Scale.;Dehiscence. Timepoint: 7th & 14 day. Method of measurement: O Michigan periodontal probe.;Clinical attachment loss. Timepoint: basleline, 22nd week. Method of measurement: O Michigan periodontal probe.;Probing pocket depth. Timepoint: basleline, 22nd week. Method of measurement: O Michigan periodontal probe.	—

Secondary

Measure	Time frame
Trismus. Timepoint: baseline,2nd,7th & 14th. Method of measurement: [(preoperative measurement postoperative measurement)/ preoperative measurement] 100%.;Facial swelling. Timepoint: baseline,2nd,7th & 14th. Method of measurement: [(postoperative measurement preoperative measurement)/preoperative measurement] 100%.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Seyed Farzad Aghdashi

Shahid Beheshti University of Medical Sciences

dr.aghdashi@gmail.com+98 21 2230 4904

Outcome results

None listed

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