NCT Number: NCT00472537
ProLOVE - Prospective Randomized Study of Midline Incisional Hernia Treatment
This purpose of this study is to compare the recovery after an operation of an incisional hernia within the limits of the rectus muscles of the abdominal wall. The use of a mesh in the repair of a postoperative hernia is considered obligatory. Placement of a retromuscular mesh is done by open or laparoscopic surgery. Focus is on the recovery phase assuming a less painful recovery after a laparoscopic procedure.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Malmö University Hospital, Department of Surgery, Malmö, Sweden
About this study
Incisional ventral hernia after abdominal surgery is a fairly common condition. In recent years the use of a prosthesis in the repair procedure has proved very effective in preventing a new hernia. A retromuscular mesh placement seems to have superior results. The mesh may be placed retromuscular through an open surgical procedure or through a laparoscopic procedure in an intra-abdominal position. Both procedures are highly standardized. A heavy weight mesh is used in the open procedure, fixed in the midline only, and a composite mesh is used intraabdominally and fixed only with titanium tackers.
SF-36 is used to assess the quality of life, and its subscale BP (bodily pain) is used as primary outcome 3 weeks postoperatively. Secondary endpoints are return to daily life, pain, complications, recurrence, patient satisfaction and cosmetic outcome.
Subjects are assessed at 1,3,8 weeks post operation and after 12 months.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Age over 18 years
- Postoperative hernias in the region of the recti abdomini muscles with a defect of less than 10 cm transversal width
- No contraindications to laparoscopic procedure
- The patient should be able to adequate ventilation/respiration after reduction of hernia contents
- Indications for elective surgery
Exclusion criteria
- Pregnant women
- Prior operation of abdominal hernia with mesh placement in the compartment of the rectus abdominus muscle (i.e. prior onlay mesh is acceptable)
- Need of an interpreter
- Current drug abuse, mental disorder or other condition which makes the patient incapable of postoperative follow up
- Body Mass index (BMI) >40
- Other planned concurrent operation
- Current oral steroid treatment, or other immune system modulating treatment
- Incarcerated incisional hernias
- Parastomal hernias
- Prior history of open abdomen
- Enterocutaneous fistula or cutaneous infection
- Hepatic cirrhosis or ascites
- Generalized malignancy
- History of radiation treatment in the abdomen.
- ASA >III
Treatment and study plan
Laparoscopic repair of midline incisional hernia
ProcedurePrimary outcomes
-
Postoperative pain recorded in SF-36
Time frame: 3 weeks after surgery
Pain measured 3 weeks after surgery in SF36 subscale Bodily Pain
Sponsors and collaborators
Lead sponsor
Skane University Hospital
Other
Collaborators
- Crafoord Foundation
- Ethicon, Inc.
- Lund University
- Region Skane
- The Anna-Lisa & Sven-Eric Lundgren Foundation, Malmö Sweden
- The Einar & Inga Nilsson Foundation
Registry information
Official study title
Prospective Randomized Evaluation of Open vs. Laparoscopic Operation of Ventral Incisional Eventrations. A Swedish Multicenter Study
Acronym: ProLOVE
Important dates
- Study start
- 2005
- Primary completion
- 2010
- Study completion
- 2010
- First posted
- May 11, 2007
- Registry last updated
- Apr 24, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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