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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02687217
Other study ID # LHMC/ECHR/2014/326
Secondary ID
Status Completed
Phase N/A
First received February 9, 2016
Last updated February 16, 2016
Start date November 2011
Est. completion date May 2013

Study information

Verified date February 2016
Source Lady Hardinge Medical College
Contact n/a
Is FDA regulated No
Health authority India: Ministry of Health
Study type Interventional

Clinical Trial Summary

The study evaluates the role of supplemental hyper-oxygenation given perioperatively on wound site infection after appendectomy. Half of the patients received ≥50% oxygen and half of them received no oxygen during the surgical procedure.


Description:

Patient with the diagnosis of acute appendicitis of >15 years of age group, with no comorbidities who presented to surgical emergency in Dr. Ram Manohar Lohia Hospital were considered for the present study.

30 patients who fulfilled the inclusion criteria and who voluntarily consented for the study were randomly allocated to the two groups- Group A (control group) and Group B (study group).

These patients were operated through Mc-Burney incision given in the right lower quadrant.

Both the groups were comparable in their demographic and preoperative profile. The study group was given ≥50% of oxygen intraoperatively and the control group was given no oxygen.

In postoperative period, oxygen was given to group A at the rate of 4 litre/minute (L/min) and group B at the rate of 6 litre/minute (L/min).

The assessment of the wound was done by using ASEPSIS (Additional treatment; Serous discharge; Erythema; Purulent exudate; Separation of deep tissues; Isolation of bacteria; and Stay) score. A score of more than 20 is considered to be infected.

Fever, raised total leucocyte count, positive pus culture, Ultrasound evidence of fluid collections, removal of sutures and duration of hospital stay were also measured for the evaluation of economic implications due to SSI.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender Both
Age group 15 Years and older
Eligibility Inclusion Criteria:

1. Clinical diagnosis or Radiological diagnosis of acute appendicitis.

2. Appendectomy through the Mc Burney incision.

Exclusion Criteria:

1. Patients with chronic obstructive pulmonary diseases.

2. Immunodeficiency disease.

3. Patients requiring midline incision.

4. Patients requiring general anaesthesia after failure of spinal anaesthesia.

5. Patients requiring higher oxygen in perioperative period.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention


Intervention

Drug:
oxygen
Hyperoxygenation refers to provision of =50% of oxygen by mask(non-rebreathing) through out the surgery.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Lady Hardinge Medical College

Outcome

Type Measure Description Time frame Safety issue
Primary ASEPSIS score ASEPSIS score- Additional treatment; Serous discharge; Erythema; Purulent exudate; Separation of deep tissues; Isolation of bacteria; and Stay. A daily score of 20 or more considered evidence of infection.
Category of infection:
Total score of 0-10 satisfactory healing; 11-20 disturbance of healing; 21-30 minor wound infection; 31-40 moderate wound infection; > 40 severe wound infection.
14 days No
Secondary Number of patients requiring additional Investigations Sonography; Pus culture; blood culture; Total Leucocyte Count. 14 days No
Secondary Number of patients requiring additional treatment Requirement of antipyretics; increased dose/ duration of antibiotic usage other than standard protocol; need for change to higher antibiotics; requirement of drainage procedures for pus/ wound infections; requirement for additional dressing sessions 14 days No
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