- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03791229
Pain and Discomfort After Appendectomy in Children
The Evaluation of Pain and Discomfort After Appendectomy in Children and Their Effects on Quality of Life
Study Overview
Status
Conditions
Detailed Description
Acute appendicitis is a diagnosis with clinical findings, laboratory tests and radiological imaging. The main pathology of appendicitis is usually the onset of the inflammatory process in the appendix vermiformis in the right lower abdomen. If untreated, the inflammatory process may progress to the perforation of the appendix and develop peritonitis. Appendectomy is an emergency surgical procedure for treatments of patients diagnosed with acute appendicitis and is the most common surgical procedure (1). Complications of appendectomy are wound site infection, postoperative intestinal adhesions and obstruction, peritonitis, bleeding, inguinal hernia, and chronic abdominal pain.
It is observed that pediatric patients who have undergone abdominal surgical procedure complained of pain and discomfort in the postoperative period (2). It should be noted that these complaints may affect quality of life. To the best of our knowledge, since there is no study in the literature, we aimed to investigate the presence of postoperative chronic abdominal pain and discomfort in children aged 8-18 years underwent appendectomy and their social and physical effects.
After Local Ethics Committee approval had been obtained, the records of children aged 8-18 years who underwent appendectomy, such as age, gender, American Society of Anesthesiology (ASA) classification score, the type of surgical procedure, and anesthetic technique were obtained from hospital information management system and anesthetic charts. Inclusion criterias were children between the ages of 8-18 years who underwent appendectomy, had ASA I physical score, and those who agree to participate for this research. Children who aged under 8 and over 18 years, had ASA II and those with higher physical score, had previously undergone surgery from the right lower abdomen, had preoperative pain complaint over 6 month, had psychiatric disorders, and whose parents do not agree to participate were excluded in this study. By calling parents, at the 6th month after the surgical procedure, the presence of chronic pain and discomfort were asked via face to face or talking on the phone. The primary endpoint of this study is to investigate the prevalence of chronic pain and discomfort at the 6th month after appendectomy in pediatric patients. The secondary endpoint is to determine the effects of chronic pain on the children's quality of life.
Pain was defined as the presence of intermittent or continuous hurtfully sensation. Discomfort was defined as an abnormal bad feeling. Children were asked whether they felt pain or discomfort while resting, coughing, and exercise. Pain was assessed using verbal numeric rating scale. Their effects on life were assessed Pediatric Quality of Life Inventory parent and child versions questionnaire at sixth months after surgery.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Adapazari
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Sakarya, Adapazari, Turkey, 54100
- Sakarya University School of Medicine Department of Anesthesiology
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Children between the ages of 8-18 years who underwent appendectomy,
- who had ASA I physical score
- who agree to participate for this research
Exclusion Criteria:
- Children who aged under 8 and over 18 years,
- who had ASA II and those with higher physical score,
- who had previously undergone surgery from the right lower abdomen,
- who had preoperative pain complaint over 6 month,
- who had psychiatric disorders,
- who do not agree to participate
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Prevalence of chronic pain
Time Frame: at the 6th month after appendectomy in pediatric patients
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The primary endpoint of this study is to investigate the prevalence of chronic pain and discomfort.
Chronic pain is going to be assessed using numeric rating scale (NRS).
The NRS for pain is a unidimensional measure of pain intensity in adults and children.
The pain NRS is a single 11-point numeric scale.
An 11-point numeric scale (NRS 11) with 0 representing one pain extreme (e.g., "nopain") and 10 representing the other pain extreme (e.g.,"pain as bad as you can imagine" and "worst pain imag-inable").
0 point represents "no pain", 1-3 "mild pain", 4-6 "moderate pain", 7-10 "severe pain".
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at the 6th month after appendectomy in pediatric patients
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
the effects of chronic pain on quality of life
Time Frame: at the 6th month after appendectomy in pediatric patients
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The secondary endpoint is to determine the effects of chronic pain on the children's quality of life.
Pediatric Quality of Life Inventory Parent and Child Versions (PedQL-P and C) is going to apply to children which report chronic pain and discomfort for evaluating their effects on quality of life.
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at the 6th month after appendectomy in pediatric patients
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Onur Palabiyik, MD, Sakarya University School of Medicine, Department of Anesthesiology
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SAU14113
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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