Colorectal DisordersNCT02116881
Incisional Hernia and Adhesion-Related Bowel Obstruction
An observational study of Colorectal Disorders and Incisional Hernia, run by The Cleveland Clinic at 1 site in United States.
Trial summary
Despite of technological advances in surgery, incisional hernia and bowel obstruction remain frequent surgical complications. To date, the relationship between these two types of surgery and the occurrence of incisional hernia remains unclear. Read more about this study
- Who is it for?
- Ages 18 to 90 yearsHealthy volunteers can take part
- Conditions the study is for
- Colorectal Disorders, Incisional Hernia, Bowel Obstruction
- What is being tested?
- Colorectal Surgery
- Type of treatment
- Surgery or procedure
- How many people
- 18 participants
- Where
- 1 siteUnited States
- Study dates
- Jan 2015to 1 Mar 2016
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 90 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Patients scheduled for an elective colorectal operation in the Department of Colorectal Surgery at Cleveland Clinic
Who may be able to join
- Age equal to or greater than 18 years
- Informed consent
- Admissions for any diagnosis that will result in colorectal surgery
- BMI lower than 50
Who cannot join
- Pregnancy
- Lack of informed consent
- Previous abdominal surgery (laparotomy/laparoscopy)
Trial locations and contacts
1 site in 1 country.
United States1 site
Cleveland Clinic Colorectal Surgery Department
Cleveland, Ohio, 44195
About this study
Official title: Incisional Hernia and Adhesion-Related Bowel Obstruction After Open and Laparoscopic Colorectal Surgery: A Prospective Cohort Study
Despite of technological advances in surgery, incisional hernia and bowel obstruction remain frequent surgical complications. To date, the relationship between these two types of surgery and the occurrence of incisional hernia remains unclear. This is an observational study to evaluate outcomes of incisional hernia with respect to the incision site and adhesion-related bowel obstruction after open and laparoscopic colorectal surgery.
Read the detailed description
The relationship between type of the approach and occurrence of incisional hernia remains unclear. This single center, prospective observational cohort study will be conducted to evaluate characteristics and outcomes of incisional hernia with regard to the impact of incision site and length and adhesion-related bowel obstruction, after open and laparoscopic colorectal surgery.
Primary endpoints
- Incisional hernia and bowel obstruction rate within two years after colorectal surgery, either clinically and/or radiologically detected.
Participants
- Patients scheduled for an elective colorectal operation will be asked for informed consent at the outpatient clinic or in the hospital on the day before surgery. All patients will be followed with a strictly controlled protocol with regard to bowel preparation, antibiotic prophylaxis, and postoperative care.
On the day of hospital discharge, patients will be asked by a blinded investigator to fill the Hospital Experience Questionnaire (HEQ).
Outpatient clinic follow-up
- Each patient will be contacted by phone call and if needed by e-mail or postal mail, concerning incisional hernia, small bowel obstruction, and Body Image Questionnaire (BIQ) at 1st, 12th and 24th months after the operation. Incisional hernia will be assessed using a validated questionnaire during phone calls. This questionnaire contains items concerning the site, treatment and recurrence of incisional hernia. And if the patient has contact with the emergency department because of complaints related to bowel obstruction among appointments, that information would also be recorded by the questionnaire. As a part of the routine care, during outpatient clinic visits related to primary disease which needed operation, these patients will be assessed by physical examination concerning incisional hernia, and BIQ at 1st, 12th and 24th months after the operation. Incisional hernia could be diagnosed clinically, or radiologically, according to symptoms reported by the patient. During these visits, patients will be asked about wound problems (infection, dehiscence, or incisional hernia) and clinical symptoms related to bowel obstruction (abdominal pain, nausea, vomiting, abdominal distention, or obstipation).
The Hospital Experience Questionnaire (HEQ) - In this questionnaire, the patients' satisfaction throughout the pre- and post-operative periods will be evaluated. The HEQ includes questions about complications, pain, length of hospital stay, time span until resumption of a normal diet, and return to daily activities (Dunker MS, Surg Endosc 1998;12:1334-40)
The Body Image Questionnaire (BIQ)
- Consists of ten items evaluating body image and cosmesis after surgery. Body image and cosmetic scales measure the patient's satisfaction with physical appearance (Dunker MS, Surg Endosc 1998;12:1334-40).
Incisional hernia is defined as "any abdominal wall gap with or without a bulge in the area of a postoperative scar perceptible or palpable by clinical examination or imaging". All sites of hernia will be considered: midline incision, Pfannenstiel (transverse), trocar site, specimen extraction site and ileostomy closure site. Incisional hernia occurring in patients in the laparoscopic group who ultimately need a laparotomy for conversion or postoperative complications within 30 days postop will be analyzed in the open group. Reoperation is defined as any return to the operating theatre (RTT) for an intra-abdominal procedure or wound complication on the index admission, or on a subsequent admission to hospital within 28 days of the initial resection. Conversion to an open operation is defined as performance of a conventional midline laparotomy, with an abdominal incision greater in size than that initially needed for specimen retrieval.
Early postoperative fascial dehiscence is distinguished from later incisional hernia, being defined by a clinically palpable gap in the abdominal fascia, with or without wound dehiscence, during the first 30 days after surgery. The distinction is made because these patients required a re-intervention, which precluded further long-term follow-up for incisional hernia.
Bowel obstruction is defined based on accepted clinical and radiologic criteria, including abdominal pain, distension, nausea, vomiting, obstipation, and distended bowel loops with air fluid levels, as evident on an abdominal X-ray.
The datasheet will be password-protected, with only the principal investigator and co-investigators having access to the information. Red-Cap (Research Electronic Data Capture) application will also be used to monitor and protect data.
Sample size calculation
- Sample size calculation was based on a study published by Duepree et al. from Cleveland Clinic in 2003 [3]. With a 2-sided significance level of 0.05 and a power of 80%, for a difference of 10% in the incidence of incisional hernia after laparoscopic and open colorectal surgery, a sample size of 140 patients per group was calculated. The number was increased to 160 patients per group upon taking into account an estimated rate of 10% of patients being lost to follow-up. Incidence of incisional hernia was expected to be 5% for the laparoscopic approach and 15% for open surgery.
Statistical Analysis
- All patients will be analyzed on an intention-to-treat basis. Significance will be determined at the p<0.05 level (2-tailed). Differences in baseline characteristics will be evaluated using Fisher's exact test for categorical variables and the Wilcoxon rank sum test for continuous or ordinal data. Using a set of preoperative and operative risk factors as independent variables and development of incisional hernia as a dependent variable, logistic regression analyses will be conducted, with the primary outcomes defined as presence of incisional hernia at incision or extraction site within 24 months of operation.
Hernia rates in relation to observation time were estimated using the Kaplan-Meier life-table method and compared via log rank test.
- Conditions
- Colorectal Disorders, Incisional Hernia, Bowel Obstruction
- Being tested
- Colorectal Surgery
- Keywords
- Incisional hernia, colorectal surgery, bowel obstruction
- Medical subject headings
- Incisional Hernia, Intestinal Obstruction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Colorectal SurgeryProcedure or surgery
Application of postoperative questionnaires will be completed by patients. The intervention is the standard of care.
| Study group | Role | What they receive |
|---|---|---|
| Open colorectal surgery | Patients scheduled to undergo open colorectal surgery from Department of Colorectal Surgery at Cleveland Clinic Receives: Procedure: Colorectal Surgery | |
| Laparoscopic colorectal surgery | Patients scheduled to undergo laparoscopic colorectal surgery from Department of Colorectal Surgery at Cleveland Clinic Receives: Procedure: Colorectal Surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
Incisional hernia
Measured: 24 month
Secondary outcomes (2)
Cosmesis
Measured: 24 month
Body image
Measured: 24 month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Apr 2014 (estimated)
- Study startJan 2015
- Primary completion1 Mar 2016
- Study completion1 Mar 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Colorectal DisordersStudies of the same condition, open and under way.
- More trials run by The Cleveland ClinicThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 18 participants (actual)
Sponsor and investigators
- Lead sponsor
- The Cleveland Clinic
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Emre Gorgun, The Cleveland Clinic
- Investigators
- Emre Gorgun, MD, Principal investigator, The Cleveland Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02116881
- Sponsor's protocol ID
- 14-261
- Status last verified
- Aug 2017
- First submitted
- 11 Apr 2014
- Last updated
- 4 Aug 2017
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Aug 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Incisional Hernia and Adhesion-Related Bowel Obstruction After Open and Laparoscopic Colorectal Surgery: A Prospective Cohort Study
- ClinicalTrials.gov ID
- NCT02116881
- Acronym / sponsor ID
- 14-261
- Conditions
- Colorectal Disorders, Incisional Hernia, Bowel Obstruction
- Keywords
- Incisional hernia, colorectal surgery, bowel obstruction
- Study type
- Observational
- Recruitment status
- Terminated
- Enrolment
- 18 participants (actual)
- Lead sponsor
- The Cleveland ClinicUniversity, hospital or other
- Study start
- Jan 2015
- Primary completion
- 1 Mar 2016 (actual)
- Study completion
- 1 Mar 2016 (actual)
- First posted
- 17 Apr 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Despite of technological advances in surgery, incisional hernia and bowel obstruction remain frequent surgical complications. To date, the relationship between these two types of surgery and the occurrence of incisional hernia remains unclear. This is an observational study to evaluate outcomes of incisional hernia with respect to the incision site and adhesion-related bowel obstruction after open and laparoscopic colorectal surgery.
Detailed description
The relationship between type of the approach and occurrence of incisional hernia remains unclear. This single center, prospective observational cohort study will be conducted to evaluate characteristics and outcomes of incisional hernia with regard to the impact of incision site and length and adhesion-related bowel obstruction, after open and laparoscopic colorectal surgery.
Primary endpoints
- Incisional hernia and bowel obstruction rate within two years after colorectal surgery, either clinically and/or radiologically detected.
Participants
- Patients scheduled for an elective colorectal operation will be asked for informed consent at the outpatient clinic or in the hospital on the day before surgery. All patients will be followed with a strictly controlled protocol with regard to bowel preparation, antibiotic prophylaxis, and postoperative care.
On the day of hospital discharge, patients will be asked by a blinded investigator to fill the Hospital Experience Questionnaire (HEQ).
Outpatient clinic follow-up
- Each patient will be contacted by phone call and if needed by e-mail or postal mail, concerning incisional hernia, small bowel obstruction, and Body Image Questionnaire (BIQ) at 1st, 12th and 24th months after the operation. Incisional hernia will be assessed using a validated questionnaire during phone calls. This questionnaire contains items concerning the site, treatment and recurrence of incisional hernia. And if the patient has contact with the emergency department because of complaints related to bowel obstruction among appointments, that information would also be recorded by the questionnaire. As a part of the routine care, during outpatient clinic visits related to primary disease which needed operation, these patients will be assessed by physical examination concerning incisional hernia, and BIQ at 1st, 12th and 24th months after the operation. Incisional hernia could be diagnosed clinically, or radiologically, according to symptoms reported by the patient. During these visits, patients will be asked about wound problems (infection, dehiscence, or incisional hernia) and clinical symptoms related to bowel obstruction (abdominal pain, nausea, vomiting, abdominal distention, or obstipation).
The Hospital Experience Questionnaire (HEQ) - In this questionnaire, the patients' satisfaction throughout the pre- and post-operative periods will be evaluated. The HEQ includes questions about complications, pain, length of hospital stay, time span until resumption of a normal diet, and return to daily activities (Dunker MS, Surg Endosc 1998;12:1334-40)
The Body Image Questionnaire (BIQ)
- Consists of ten items evaluating body image and cosmesis after surgery. Body image and cosmetic scales measure the patient's satisfaction with physical appearance (Dunker MS, Surg Endosc 1998;12:1334-40).
Incisional hernia is defined as "any abdominal wall gap with or without a bulge in the area of a postoperative scar perceptible or palpable by clinical examination or imaging". All sites of hernia will be considered: midline incision, Pfannenstiel (transverse), trocar site, specimen extraction site and ileostomy closure site. Incisional hernia occurring in patients in the laparoscopic group who ultimately need a laparotomy for conversion or postoperative complications within 30 days postop will be analyzed in the open group. Reoperation is defined as any return to the operating theatre (RTT) for an intra-abdominal procedure or wound complication on the index admission, or on a subsequent admission to hospital within 28 days of the initial resection. Conversion to an open operation is defined as performance of a conventional midline laparotomy, with an abdominal incision greater in size than that initially needed for specimen retrieval.
Early postoperative fascial dehiscence is distinguished from later incisional hernia, being defined by a clinically palpable gap in the abdominal fascia, with or without wound dehiscence, during the first 30 days after surgery. The distinction is made because these patients required a re-intervention, which precluded further long-term follow-up for incisional hernia.
Bowel obstruction is defined based on accepted clinical and radiologic criteria, including abdominal pain, distension, nausea, vomiting, obstipation, and distended bowel loops with air fluid levels, as evident on an abdominal X-ray.
The datasheet will be password-protected, with only the principal investigator and co-investigators having access to the information. Red-Cap (Research Electronic Data Capture) application will also be used to monitor and protect data.
Sample size calculation
- Sample size calculation was based on a study published by Duepree et al. from Cleveland Clinic in 2003 [3]. With a 2-sided significance level of 0.05 and a power of 80%, for a difference of 10% in the incidence of incisional hernia after laparoscopic and open colorectal surgery, a sample size of 140 patients per group was calculated. The number was increased to 160 patients per group upon taking into account an estimated rate of 10% of patients being lost to follow-up. Incidence of incisional hernia was expected to be 5% for the laparoscopic approach and 15% for open surgery.
Statistical Analysis
- All patients will be analyzed on an intention-to-treat basis. Significance will be determined at the p<0.05 level (2-tailed). Differences in baseline characteristics will be evaluated using Fisher's exact test for categorical variables and the Wilcoxon rank sum test for continuous or ordinal data. Using a set of preoperative and operative risk factors as independent variables and development of incisional hernia as a dependent variable, logistic regression analyses will be conducted, with the primary outcomes defined as presence of incisional hernia at incision or extraction site within 24 months of operation.
Hernia rates in relation to observation time were estimated using the Kaplan-Meier life-table method and compared via log rank test.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Open colorectal surgery | – | Procedure: Colorectal SurgeryPatients scheduled to undergo open colorectal surgery from Department of Colorectal Surgery at Cleveland Clinic |
| Laparoscopic colorectal surgery | – | Procedure: Colorectal SurgeryPatients scheduled to undergo laparoscopic colorectal surgery from Department of Colorectal Surgery at Cleveland Clinic |
Who may qualify
- Ages
- 18 to 90 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Patients scheduled for an elective colorectal operation in the Department of Colorectal Surgery at Cleveland Clinic
Key inclusion criteria (4 listed)
- Age equal to or greater than 18 years
- Informed consent
- Admissions for any diagnosis that will result in colorectal surgery
- BMI lower than 50
Key exclusion criteria (3 listed)
- Pregnancy
- Lack of informed consent
- Previous abdominal surgery (laparotomy/laparoscopy)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Colorectal SurgeryApplication of postoperative questionnaires will be completed by patients. The intervention is the standard of care. | Procedure or surgery | Laparoscopic colorectal surgery, Open colorectal surgery |
Primary outcome
Incisional hernia
Time frame: 24 month
2 secondary outcomes
Cosmesis
Time frame: 24 month
Body image
Time frame: 24 month
Results and safety
The study was stopped early. Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Aug 2017.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Emre Gorgun, MD principal investigator
The Cleveland Clinic
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Colorectal Disorders and Incisional Hernia, run by The Cleveland Clinic at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 4 Aug 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early. Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Incisional hernia (time frame: 24 month). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Aug 2017.