Randomized Controlled Trial Comparing Drains Usage vs Without Drains After Thyroid Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorAssiut University

About this trial

The aim of this study is to compare patients who used drain to patients who did not use drain post-thyroidectomy regarding the short-term outcomes .

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

(1) Male or female patients undergoing thyroidectomy (2) Patients with ages: from 18 to 60 years old. (3) Patients with normal thyroid function tests (4) Patients who are fit for general-anesthesia.

Disqualifiers

(1) Patients with bleeding diathesis and those on anticoagulants. (2) Patients with thyrotoxicosis (uncontrolled) (3) Patients those requiring neck L.N dissection. (4) Patients with previous neck surgeries. (5) Patients with severe comorbid conditions with high risk for general anesthesia.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Suction Drain placement (Example: Q-vac)

    Device

    After thyroid surgery we pust drain at bed of surgery to monitor post operative bleeding.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Group drain (A)Active comparator 1 intervention
Group B: Group no drain (B)No intervention 0 interventions

Trial outcomes

Primary outcomes

1

Rate of hematoma post-operative .

Rate of post operative hematoma formation and effect of drain in preventing it

Time frame
24 hours

Secondary outcomes

1

Rate of infection

Compare Rate of surgical site infection between two groups

Time frame
7 days
2

Rate of re intervention

Time frame
7 days
3

Post-operative pain by visual analogue scale

Time frame
3 days
4

Post-operative hospital stay in days

Length of hospital stay: described as the length of a single hospitalization, which is determined by subtracting the day of admission from the day of discharge. Data are collected from patients underwent thyroid surgery using a pretested, structured interviewer-administered questionnaire, medical record review,

Time frame
7 days

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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