Anterior Transversalis Fascia Approach Versus Preperitoneal Space Approach for Inguinal Hernia Repair in Residents
Primary Purpose
Inguinal Hernia
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Anterior transversalis fascia approach
Preperitoneal space approach
Sponsored by
About this trial
This is an interventional treatment trial for Inguinal Hernia focused on measuring anterior transversalis fascia repair; preperitoneal repair
Eligibility Criteria
Inclusion Criteria:
- Diagnosed with primary unilateral inguinal hernia
- Aged 18-80 years
- American Society of Anesthesiologists (ASA) classification I-II
- Provision of informed consent
Exclusion Criteria:
- Severe organ dysfunction or inability to tolerate surgery
- Hernia recurrence
- Giant hernia (inner size of the hernia > 4 cm)
- Scrotal hernia
- Incarcerated inguinal hernia
- Inability to complete follow-up or questionnaire because of mental disorder or other reasons
- History of preperitoneal surgery, such as radical prostatectomy
Sites / Locations
- General Hospital of Benxi Steel and Iron (Group) Co., LTDRecruiting
- The First Affiliated Hospital of Dalian Medical UniversityRecruiting
- The First Hospital of Dandong CityRecruiting
- The First Affiliated Hospital of Jinzhou Medical UniversityRecruiting
- The 202nd Hospital of PLARecruiting
- Fengtian Hospital of Shenyang Medical CollegeRecruiting
- General Hospital of Shenyang Military RegionRecruiting
- The Fourth Affiliated Hospital of China Medical UniversityRecruiting
- Shengjing Hospital of China Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
anterior transversalis fascia approach
preperitoneal space approach
Arm Description
Patients with inguinal hernia will undergo inguinal hernia repair via the anterior transversalis fascia approach.
Patients with inguinal hernia will undergo inguinal hernia repair via the preperitoneal space approach.
Outcomes
Primary Outcome Measures
VAS pain score
Visual Analogue Scale(VAS) pain score is one of the most commonly used tools for assessing pain.It comprises a 10 cm line with 0 at one end, representing no pain, and 10 at the other end, representing the worst pain imaginable; the patient places a mark on the line to indicate the degree of pain that they are experiencing.
Secondary Outcome Measures
Postoperative complications
Postoperative complications including wound infection, rates of hematoma, seroma, hernia recurrence, intestinal obstruction, intestinal fistula, entocele, mesenteric thrombosis, femoral vein thrombosis, ischemic orchitis, painful ejaculation, varicocele and scrotal edema.
Full Information
NCT ID
NCT02984917
First Posted
December 1, 2016
Last Updated
June 14, 2017
Sponsor
The Fourth Affiliated Hospital of China Medical University
1. Study Identification
Unique Protocol Identification Number
NCT02984917
Brief Title
Anterior Transversalis Fascia Approach Versus Preperitoneal Space Approach for Inguinal Hernia Repair in Residents
Official Title
Anterior Transversalis Fascia Approach Versus Preperitoneal Space Approach for Inguinal Hernia Repair in Residents in Northern China: a Prospective, Multi-center, Randomized, Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 6, 2017 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
June 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Fourth Affiliated Hospital of China Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To investigate the advantages and disadvantages of the anterior transversalis fascia approach versus the preperitoneal approach for inguinal hernia repair in residents from northern China regarding common postoperative complications (including acute and chronic pain, wound infection, rates of wound infection, hematoma, seroma, and hernia recurrence) and severe postoperative complications.
Detailed Description
History and current related studies Inguinal hernia is a common surgical disease that manifests as protrusion of abdominal cavity contents through the inguinal canal because of an abdominal wall defect. It is more common in males than in females, with an overall incidence of 5-10%. Methods for surgical repair of abdominal wall defects in the inguinal region are classified as either 'tension'repairs or 'tension-free' repairs. Herniorrhaphy through repair of the posterior wall of the inguinal canal was first described by Bassini in 1887, and is regarded as a classic surgical method.
As understanding of the anatomic location and pathophysical characteristics of inguinal hernia developed, the American surgeon Lichtenstein proposed a new concept of tension-free herniorrhaphy. This technique was quickly adopted worldwide because of its advantages including minimal invasion, technical ease, effectiveness, low complication rate, low recurrence rate, and allowance of resumption of unrestricted physical activity. The most common technique is open tension-free herniorrhaphy.
Many surgical repair methods involving patches (of varying types and materials) are available for inguinal hernia repair.
Tension-free herniorrhaphy methods include anterior transversalis fascia repair, preperitoneal repair, abdominal cavity patch repair and combined repair approaches. Lichtenstein herniorrhaphy is the representative technique of anterior transversalis fascia repair. Preperitoneal repair techniques include transabdominal preperitoneal, total extraperitoneal, and Kugel repair techniques. The combined repair approaches refer to tension-free herniorrhaphy using a modified Kugel patch and the Ultrapro hernia system.
There are few reports on the effects of different inguinal hernia repair approaches on postoperative complications, particularly regarding severe postoperative complications, in patients in northern China. The incidence of severe complications after inguinal hernia repair is relatively low, but this surgery can lead to physical impairment or organ dysfunction that greatly decreases patient quality of life and places a heavy burden on the patient's family and society. At present, there is a scarcity of clinical evidence from large-sample, randomized, controlled trials investigating the effectiveness of inguinal hernia repair via the anterior transversalis fascia approach versus the preperitoneal approach.
Adverse events and serious adverse events (SAE) According to the study protocol and clinical judgment, AE/SAE occurring after herniorrhaphy will be reported to the Department of General Surgery, the Fourth Affiliated Hospital of China Medical University.
AE refer to any adverse medical events occurring after herniorrhaphy in patients or clinical subjects. SAE refer to any adverse postoperative medical events involving one or more of the following criteria:
Death, irrespective of the cause Life-threatening event Severe or permanent disability or organ dysfunction Hemorrhage Malformation, birth defect Hospitalization or extended hospital stay Re-admission to hospital Recurrence (symptomatic) of inguinal hernia
Statistical analysis Descriptive statistics will be used to analyze the data. For measurement data, the number of patients (number of missing patients), mean, median, standard deviation, first quartile, third quartile, and maximum and minimum will be described, and 95% confidence intervals will be calculated. For counted data, the frequency and relative numbers will be described, and 95% confidence intervals will be calculated. According to whether the differences between scores before and after treatments are normally distributed, the paired t-test or Wilcoxon signed rank test will be used for comparison of measurement data in the same group. The chi-squared test or Fisher's exact test will be used for analysis of counted data, and the Wilcoxon signed rank test will be used for analysis of ranked data. The last-observation-carried-forward imputation method will be used when the effects-related visit data at the last visit are missing.
Full analysis set According to the intention-to-treat principle, patients who receive at least one treatment according to study protocol and undergo at least one evaluation regarding curative effects after baseline evaluation will be included in the full analysis set.
Curative effects analysis Full analysis set analysis of curative effects will be performed. The proportions of patients with no complications, patients with common complications, and patients with severe complications within postoperative 3 weeks will be analyzed using descriptive statistics. The chi-squared test or Fisher's exact test will be used for comparison of differences between groups. If statistical differences exist between groups, the Bonferroni method will be used to adjust the α value, and pairwise comparisons will be made.
If the change in VAS pain score after treatment meets the normality and homogeneity of variance, analysis of variance will be performed. If the statistical analysis of variance results are significant, in-depth statistical analysis will be performed, and the Bonferroni method will be used for pairwise comparisons. Otherwise, the Kruskal-Wallis test will be performed. If the statistical results of the Kruskal-Wallis test are significant, in-depth statistical analysis will be performed, and the independent Wilcoxon signed rank test will be performed. The Bonferroni method will be used to adjust P values for pairwise comparisons.
Safety evaluation Safety analysis and analysis of the incidence of postoperative complications will be performed using descriptive statistics. The chi-squared test or Fisher's exact test will be performed for comparisons between groups. If significant differences exist, the Bonferroni method will be used to adjust the α value, and in-depth pairwise comparisons will be made between groups. Vital signs and laboratory outcomes will be analyzed using descriptive statistics. The paired t-test or Wilcoxon signed rank test will be used to analyze the differences between values before and after surgery. Imaging data and electrocardiograms will be analyzed using cross tabulations.
Economic analysis Cost-utility analysis will be used for economic evaluation, and sensitivity analysis of cost and utility will be performed.
Interim analysis When an adequate number of patients are enrolled and followed-up, interim analysis will be performed. When data are included for the full analysis set and recorded in the database, the first interim analysis during the management period will be performed to check whether the core data collected are suitable for preliminary significant data analysis. According to research progression, subsequent interim analysis of all data included in the database will then be designated. After acquiring approval from the Department of General Surgery and Scientific Construction Committee, the Fourth Affiliated Hospital of China Medical University, the data collected in the Department of General Surgery, the Fourth Affiliated Hospital of China Medical University are likely to be analyzed together with the data collected from the other research centers. In accordance with applicable laws and regulations, the information on the subjects in the study will be kept confidential. The data for interim analysis will be precisely described in a statistical analysis plan. The interim analysis results will be submitted to the sponsor and the project manager in the form of a statistical analysis report, and as slides by the co-sponsors.
Sample size Investigators hypothesized that anterior transversalis fascia repair can reduce the percentage of patients with postoperative pain by 15% compared with the percentage of patients with pain before surgery. Taking α = 0.05 and power = 80%, the final effective sample size of n = 300 was calculated. Assuming a patient loss rate of 20%, investigators require 360 patients. This study is planned to be performed in more than nine institutes to investigate the effectiveness of inguinal hernia repair via the anterior transversalis fascia approach versus the preperitoneal approach in patients in northern China. Investigators plan to include at least 2,000 patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inguinal Hernia
Keywords
anterior transversalis fascia repair; preperitoneal repair
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
2000 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
anterior transversalis fascia approach
Arm Type
Experimental
Arm Description
Patients with inguinal hernia will undergo inguinal hernia repair via the anterior transversalis fascia approach.
Arm Title
preperitoneal space approach
Arm Type
Experimental
Arm Description
Patients with inguinal hernia will undergo inguinal hernia repair via the preperitoneal space approach.
Intervention Type
Procedure
Intervention Name(s)
Anterior transversalis fascia approach
Intervention Description
Patients will undergo inguinal hernia repair via the anterior transversalis fascia approach.
Intervention Type
Procedure
Intervention Name(s)
Preperitoneal space approach
Intervention Description
Patients will undergo inguinal hernia repair via the preperitoneal space approach.
Primary Outcome Measure Information:
Title
VAS pain score
Description
Visual Analogue Scale(VAS) pain score is one of the most commonly used tools for assessing pain.It comprises a 10 cm line with 0 at one end, representing no pain, and 10 at the other end, representing the worst pain imaginable; the patient places a mark on the line to indicate the degree of pain that they are experiencing.
Time Frame
changes of month 1, month 3, month 12, month 24 after operation
Secondary Outcome Measure Information:
Title
Postoperative complications
Description
Postoperative complications including wound infection, rates of hematoma, seroma, hernia recurrence, intestinal obstruction, intestinal fistula, entocele, mesenteric thrombosis, femoral vein thrombosis, ischemic orchitis, painful ejaculation, varicocele and scrotal edema.
Time Frame
changes of month 1, month 3, month 12, month 24 after operation
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosed with primary unilateral inguinal hernia
Aged 18-80 years
American Society of Anesthesiologists (ASA) classification I-II
Provision of informed consent
Exclusion Criteria:
Severe organ dysfunction or inability to tolerate surgery
Hernia recurrence
Giant hernia (inner size of the hernia > 4 cm)
Scrotal hernia
Incarcerated inguinal hernia
Inability to complete follow-up or questionnaire because of mental disorder or other reasons
History of preperitoneal surgery, such as radical prostatectomy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hangyu Li, Ph.D
Phone
8618940257002
Email
li_hangyu@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hangyu Li, Ph.D
Organizational Affiliation
The Fourth Affiliated Hospital of China Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
General Hospital of Benxi Steel and Iron (Group) Co., LTD
City
Benxi
State/Province
Liaoning
ZIP/Postal Code
117000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhong-shu Dai, Ph.D
Phone
8613841460709
Email
dzs20092009@163.com
First Name & Middle Initial & Last Name & Degree
Zhong-shu Dai, Ph.D
Facility Name
The First Affiliated Hospital of Dalian Medical University
City
Dalian
State/Province
Liaoning
ZIP/Postal Code
116011
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
De-wei An, Ph.D
Phone
8613704262820
Email
anweide@sina.com
First Name & Middle Initial & Last Name & Degree
De-wei An, Ph.D
Facility Name
The First Hospital of Dandong City
City
Dandong
State/Province
Liaoning
ZIP/Postal Code
118000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yao-qiang Wu, Ph.D
Phone
8613704959939
Email
wuyaoqiang@sina.com
First Name & Middle Initial & Last Name & Degree
Yao-qiang Wu, Ph.D
Facility Name
The First Affiliated Hospital of Jinzhou Medical University
City
Jinzhou
State/Province
Liaoning
ZIP/Postal Code
121001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shi-feng Qiao, Ph.D
Phone
8618004969133
Email
shifengqiao2013@163.com
First Name & Middle Initial & Last Name & Degree
Shi-feng Qiao, Ph.D
Facility Name
The 202nd Hospital of PLA
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fu-rong Wang, Ph.D
Phone
8613352457285
Email
furong_jiyu@126.com
First Name & Middle Initial & Last Name & Degree
Fu-rong Wang, Ph.D
Facility Name
Fengtian Hospital of Shenyang Medical College
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110024
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shao-jun Zhang, Ph.D
Phone
8613909888012
Email
shaojunzhang@163.com
First Name & Middle Initial & Last Name & Degree
Shao-jun Zhang, Ph.D
Facility Name
General Hospital of Shenyang Military Region
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110031
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hui-yong Jiang, Ph.D
Phone
8613352457673
Email
huiyongj@126.com
First Name & Middle Initial & Last Name & Degree
Hui-yong Jiang, Ph.D
Facility Name
The Fourth Affiliated Hospital of China Medical University
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hang-yu Li, Ph.D
Phone
8618940257002
Email
li_hangyu@126.com
First Name & Middle Initial & Last Name & Degree
Hang-yu Li, Ph.D
Facility Name
Shengjing Hospital of China Medical University
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
117004
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fu-quan Yang, Ph.D
Phone
8618940251755
Email
yangfq@sj-hospital.org
First Name & Middle Initial & Last Name & Degree
Fu-quan Yang, Ph.D
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
28860228
Citation
Fan Q, Zhang DW, Yang DY, Li HW, Wei SB, Yang L, Yang FQ, Zhang SJ, Wu YQ, An WD, Dai ZS, Jiang HY, Wang FR, Qiao SF, Li HY. Anterior transversalis fascia approach versus preperitoneal space approach for inguinal hernia repair in residents in northern China: study protocol for a prospective, multicentre, randomised, controlled trial. BMJ Open. 2017 Aug 31;7(8):e016481. doi: 10.1136/bmjopen-2017-016481.
Results Reference
derived
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Anterior Transversalis Fascia Approach Versus Preperitoneal Space Approach for Inguinal Hernia Repair in Residents
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