Complications in Body Contouring Surgery

Status Enrolling by invitation

Clinical Trial Summary

The objective of this study is to describe the wound related complication rate in post-bariatric body contouring surgery patients who are treated according to the new Dutch guideline and to asses the factors associated with a higher complication rate.

Clinical Trial Description

In the recently published guideline of the Dutch Association of Plastic Surgeons it is advised that assessment and improvement of the nutritional status should be part of pre-operative work-up of all post-bariatric patients who undergo body contouring surgery (BCS). The assessment should consist of consultation of a dietician and measurement of the nutritional parameters associated with wound healing. It is advised to assess the following parameters:

- albumin

- hemoglobin

- vitamin D (25-hydroxy vitamin D)

- ferritin

- folic acid

- vitamin B12

Standard treatment in this study will consist of the pre-operative work-up as advised by the guideline. Participants will have a consultation with the dietician to assess (protein) intake. In addition the first blood sample, which is part of standard treatment according to the new protocol, will be obtained to assess foregoing parameters. If there are nutritional deficiencies they will be treated according to the protocol of the department of Bariatric Surgery of the treating hospital.

To evaluate the effect of the treatment of deficiencies and to be sure that there are no deficiencies present during the BCS a second blood sample will be drawn during the body contouring procedure. For study purposes this second sample will be collected in all patients, even if a deficiency was not present at the first blood sample.

The dietician will assess current intake of the patients, with special attention the protein intake. Based on guidelines on protein-intake in post-bariatric patients and after consultation of experts (Dieticians of Maastricht University) investigators decided that the aim of the minimum protein intake is 1.5 gram per kilogram bodyweight (calculated with BMI 27kg/m2) per day. The first consultation at the dietician will be eight weeks prior to surgery. Patients will be advised to start with the extra protein-intake four weeks prior to surgery and continue this until the wounds are completely healed.

Six weeks after surgery a questionnaire will be handed-out to the patients, to assess the compliance to the treatment regime. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02552433
Study type	Observational [Patient Registry]
Source	St. Antonius Hospital
Contact
Status	Enrolling by invitation
Phase
Start date	September 2015
Completion date	September 2019

View Details

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT04517591` - Reducing Sedentary Time in Bariatric: The Take a STAND for Health Study	N/A
Active, not recruiting	`NCT04433338` - The PREBA Study: Effect of Preoperative Weight Loss With a 14-day Low-calorie Diet on Surgical Procedure and Outcomes in Patients Undergoing RYGB Surgery	N/A
Completed	`NCT05854875` - Diabetes Remission After RYGBP and RYGBP With Fundus Resection	N/A
Recruiting	`NCT06460233` - Blood Pressure Changes After Bariatric Surgery
Completed	`NCT00535600` - Effects of Bariatric Surgery on Insulin
Withdrawn	`NCT04771247` - Endoscopic Cardiac Band Ligation for the Management of Refractory GERD After Laparoscopic Sleeve Gastrectomy	N/A
Not yet recruiting	`NCT03203161` - Registry on Obesity Surgery in Adolescents
Completed	`NCT02525016` - Safety Profile of IntRAvenous Lidocaine Use in Coelioscopic Bariatric Surgery	Phase 3
Recruiting	`NCT01984762` - Sleeve Gastrectomy and Roux-en-Y Gastric Bypass in the Treatment of Type 2 Diabetes Mellitus.	N/A
Not yet recruiting	`NCT01652105` - Randomized Trial of Preoperative Diets Before Bariatric Surgery	N/A
Completed	`NCT00989157` - Effects of Gastric Bypass on Blood Levels of Duloxetine	Phase 3
Completed	`NCT03609632` - Understanding Hypoglycaemia After Bariatric Surgery	N/A
Completed	`NCT05454696` - Online Clinic Pilates Exercises in Patients Undergoing Bariatric Surgery	N/A
Completed	`NCT04040647` - Tolerance of Early Postoperative Mobilization and Ambulation
Recruiting	`NCT04297306` - Virtual Reality Exercise Gaming in Patients Awaiting Bariatric Surgery	N/A
Recruiting	`NCT05428618` - Mobile Application for Bariatric Surgery Patients	N/A
Not yet recruiting	`NCT03975244` - Semi-supervised Exercise Program Before Bariatric Surgery	N/A
Not yet recruiting	`NCT03900481` - Use of an Endoluminal-suturing Device for Endoscopic Gastric Reduction as an Aid for Class I Obesity, or Class II Obesity Without Comorbidity	N/A
Recruiting	`NCT06157606` - Prediction Model for Inadequate Weight Loss After Sleeve Gastrectomy
Recruiting	`NCT06218953` - The Impact of Preoperative Anemia on Postoperative Anemia and Related Nutrient Abnormalities After Bariatric Surgery

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Complications in Body Contouring Surgery — CONTOUR

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms