Hernia, Ventral Clinical Trial
Official title:
Prospective Observational Trial of Initial Non-operative Management of Ventral Hernia Repair
Verified date | April 2018 |
Source | The University of Texas Health Science Center, Houston |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Ventral hernias are among the most common surgical diseases among patients.The natural history of patients with ventral hernias who are managed non-operatively is unknown. The aim of this prospective trial is to document the natural history of patients who are undergoing initially non-operative management. The investigators hypothesize that 1) the risk of emergency ventral hernia repair is low, 2) the risk of elective ventral hernia repair is high, and 3) patients managed non-operatively will develop increasing hernia size and symptom progression. This is a prospective observational study of all patients undergoing non-operative management at LBJ General Hospital. Patients will be consented and then followed for 5 years. Phone interviews will be done with these patients yearly to assess surgical and medical history, information about their hernia, including pain level due to the hernia, as well as function and quality of life.
Status | Active, not recruiting |
Enrollment | 143 |
Est. completion date | June 2020 |
Est. primary completion date | June 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - All patients undergoing initial non-operative management as chosen by current practice patterns - All patients who opt for non-operative management due to personal choice, lack of symptoms or concerns regarding surgical risks. - Age 18 or older Exclusion Criteria: - Patient meets surgery criteria but elects for surgery within 1 year due to personal scheduling - Patient smokes < 1 pack per day, is actively quitting smoking, and desires to follow-up within 3 months upon smoking cessation - Patient with BMI < 35 kg/m2, is actively losing weight, and desires to follow-up within 3 months upon weight loss goals being met - Patient is unlikely to be able to follow-up due to no personal or home phone - Patient is enrolled in another trial |
Country | Name | City | State |
---|---|---|---|
United States | LBJ General Hospital-UT Health | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
The University of Texas Health Science Center, Houston |
United States,
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Fitzgibbons RJ Jr, Ramanan B, Arya S, Turner SA, Li X, Gibbs JO, Reda DJ; Investigators of the Original Trial. Long-term results of a randomized controlled trial of a nonoperative strategy (watchful waiting) for men with minimally symptomatic inguinal hernias. Ann Surg. 2013 Sep;258(3):508-15. doi: 10.1097/SLA.0b013e3182a19725. — View Citation
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in pain from baseline using the Visual Analog Scale for Pain | Once a year for 5 years | ||
Other | Change in patient function from baseline using the HerQLes Survey | Once a year for 5 years | ||
Other | Change in patient quality of life from baseline using the HerQLes Survey | Once a year for 5 years | ||
Other | Change in hernia size based on clinical exam or CT scan | Once a year for 5 years | ||
Primary | Rate of surgical repair of the ventral hernias per patient year | Once a year for 5 years | ||
Secondary | Rate of emergency repair of ventral hernias per patient year | Once a year for 5 years | ||
Secondary | Rate of elective repair of ventral hernias per patient year | Once a year for 5 years | ||
Secondary | Rate of emergency room visits per patient year | Once a year for 5 years |
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