Comparison of Two Different Suture Knot Techniques on Post-Operative Trismus and Swelling After Impacted Third Molar Surgery

ConditionsTrismusSwelling
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeUp to 45
SponsorWatim Medical & Dental College

About this trial

To compare the two different suture knot techniques, locked and unlocked, in terms of mean on postoperative trismus and swelling after impacted mandibular third molar surgery.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

• Healthy individuals

Gender: male and female

Age: 18-45 years

Mandibular third molar impaction all positions

Disqualifiers

• Patients with ASA status III and above

Patients requiring multiple extractions in same appointment

Patients allergic to Lignocaine

Patients in whom adrenaline is contraindicated

Trial design

Design model

Parallel

Treatments tested in this trial

  • locking and non locking suture techniques

    Procedure/Surgery

    The participating patients will be randomly assigned into two groups, i.e. receiving locked (L) or unlocked (UL) sutures, using a lottery method. Equal patients will be assigned in both groups. In group L (Locked suturing), the flap will be repositioned and sutured with the locked technique (straight-reverse-straight) hermetically using 3-0 black silk. In group UL (Unlocked suturing), the flap will be repositioned and sutured with the unlocked technique (three straight knots) loosely using 3-0 black silk. Demographic details (including name, age, gender, contact) will be obtained and recorded on specific data collection forms. On the day of surgery before the surgery commences, measurements will be taken for trismus and swelling which will be entered on the data collection form. Trismus will be evaluated by measuring the distance between the mesio-incisal corners of the upper and lower right central incisors at maximum mouth opening in mm, using Castroviejo instrument. The facial swel

  • non locking suture technique

    Procedure/Surgery

    The participating patients will be randomly assigned into two groups, i.e. receiving locked (L) or unlocked (UL) sutures, using a lottery method. Equal patients will be assigned in both groups. In group L (Locked suturing), the flap will be repositioned and sutured with the locked technique (straight-reverse-straight) hermetically using 3-0 black silk. In group UL (Unlocked suturing), the flap will be repositioned and sutured with the unlocked technique (three straight knots) loosely using 3-0 black silk. Demographic details (including name, age, gender, contact) will be obtained and recorded on specific data collection forms. On the day of surgery before the surgery commences, measurements will be taken for trismus and swelling which will be entered on the data collection form. Trismus will be evaluated by measuring the distance between the mesio-incisal corners of the upper and lower right central incisors at maximum mouth opening in mm, using Castroviejo instrument.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: locking sutureExperimental treatment 2 interventions
Group B: non locking sutureExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

effect of locking and non locking suture technique on trismus

Trismus will be evaluated by measuring the distance between the mesio-incisal corners of the upper and lower right central incisors at maximum mouth opening in mm, using Castroviejo instrument.

Time frame
3 days and 7 days post operatively
2

Effect of locking and unlocking sutures on facial swelling

The facial swelling in cm will be determined by measuring the distance from the corner of the mouth to the attachment of the earlobe following the bulge of the cheek and the distance from the outer canthus of the eye to the angle of the mandible using a plastic measuring tape.

Time frame
Post operative day three and day seven

Secondary outcomes

Other outcomes

Sponsors and contacts

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