Anorectal MalformationsNCT04901819
Longterm Outcomes of Individuals With Anorectal Malformations
An observational study of Anorectal Malformations, run by Karolinska Institutet at 1 site in Sweden.
Trial summary
This is a cross-sectional observational study with the aim to assess longterm outcomes in a large cohort of individuals with anorectal malformations. Patients managed for anorectal malformations at Karolinska University Hospital, Stockholm, Sweden, Stockholm 1994-2017 will be reviewed and they will be invited to… Read more about this study
- Who is it for?
- Ages 4 to 28 years
- Conditions the study is for
- Anorectal Malformations
- How many people
- 300 participants
- Where
- 1 siteSweden
- Study dates
- 1 Jan 2022to 31 Jul 2023
- 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 4 to 28 years
- All sexes
- No healthy volunteers
- Child, Adult
Study population: Individual who have undergone surgical management for anorectal malformations at Karolinska University Hospital, Stockholm, Sweden from 1994 to 2017.
Who may be able to join
- Individual who has undergone surgical management for anorectal malformation at Karolinska University Hospital 1994 to 2017.
Who cannot join
- Individual not providing informed consent.
Trial locations and contacts
1 site in 1 country.
About this study
This is a cross-sectional observational study with the aim to assess longterm outcomes in a large cohort of individuals with anorectal malformations. Patients managed for anorectal malformations at Karolinska University Hospital, Stockholm, Sweden, Stockholm 1994-2017 will be reviewed and they will be invited to respond to validated questionnaires evaluating bowel function (>4 years of age), urinary tract function (>4 years of age), sexual function (>18 years of age) and quality of life (>8 years of age). Data will be analyzed with descriptive and comparative statistics.
Read the detailed description
Background Anorectal malformations comprise a spectrum of congenital anomalies, that range from mild anterior displacement of the anus to very complex anomalies, involving both the hindgut and the urogenital tract. The birth prevalence in Sweden is approximately 1:3000 (1). Associated anomalies are encountered in 50-60 % of individuals with anorectal malformation. Anorectal malformations are associated with tethered cord in 20-30% of patients, which may impair bowel and urinary tract function. Development of surgical techniques and neonatal care have improved survival of children with anorectal malformations over the last decades. The focus of care has shifted from survival to optimizing bowel and urinary tract function as well as reducing the negative impact on quality of life. Current surgical techniques were introduced during the early 1980's. The outcomes compare favorably with older techniques, although there is still limited information on the outcomes up to adult age. Particularly, there are limited data of composite outcomes of bowel function, urinary tract function, sexual function and quality of life in comparison to age- and gender-matched controls from the normal population. Newborn infants are often screened for tethered cord with ultrasound. It is unclear if infants with normal ultrasound also need an MRI at a later stage to exclude spinal cord anomalies. Tethered cord is frequently asymptomatic. There are conflicting data with respect to prophylactic de-tethering.
Aims The overall aim of this project was to assess composite outcomes, bowel function, urinary tract function, sexual function, and quality of life in a cross-sectional study of children with ARM managed at Karolinska University Hospital.
Specific aims
- To assess if bowel function, urinary tract function, sexual function, and quality of life is impaired in children with ARM compared with normative data.
- To assess if bowel function, urinary tract function, sexual function and quality of life correlate
- To assess if individuals with ARM and tethered cord benefit from detethering.
- To assess if ultrasound of the spinal cord and MRI are equal imaging modalities to diagnose tethered cord.
Methods Study design Cross-sectional observational study. The STROBE Statement for reporting of observational studies will be used (2).
Settings and participants All individuals managed for an anorectal malformation at Karolinska University Hospital from 1994 to 2017 will be eligible for the study. Patients and/or parents who provide informed consent and fill in the questionnaires will be included in the study. There will be 300-400 eligible patients.
Data sources and variables Demographic and clinical details will be recorded retrospectively from the medical records, including gender, birth weight, gestational age, associated syndromes and anomalies, family history, presenting symptoms, type of ARM, surgical details including postoperative complications and re-operations. Questionnaires will be sent according to age to the participants to assess bowel function, urinary tract function, sexual function, and quality of life. Questionnaires on sexual function and quality of life will not be sent to individuals with intellectual impairment, eg. Down syndrome. It will be possible to respond to the questionnaires using a digital platform. Bowel function will be assessed in individuals more than 4 years of age using a bowel function score (BFS) questionnaire (3) developed for assessment of bowel function in pediatric anorectal disorders and validated in patients and in the general Finnish population (4). Urinary tract function will be assessed in individuals more than 4 years of age with a questionnaire on lower urinary tract symptoms, with questions addressing history of urinary tract infection, urgency, urge incontinence, stress incontinence, straining to begin urination, and leakage of urine without physical activity or apparent need to urinate, based on items adapted from the previously validated Danish Prostatic Symptom Score. Profile of Sexual Female function will be used to assess sexual function in the female patients more than 18 years of age. IIEF will be used to assess sexual function in males more than 18 years of age. KIDSCREEN, a validated instrument assessing children's and adolescents subjective health and well-being, will be used to assess the quality of life in children and adolescents 8 to 18 years of age. In patients more than 18 years old, Psychological general well-being index (PGWB) will be used to assess quality of life. In a sub-study, individuals with tethered cord will be identified. The outcomes among patients with tethered cord who have undergone de-tethering will be compared with those who have not undergone an operation. In a second sub-study, spinal cord ultrasound and MRI images will be reviewed by two experienced pediatric radiologists in a blinded fashion. Correlation between the two imaging modalities will be analyzed.
Data analysis Pseudonymized data will be recorded in Excel spread sheets. Data will be analyzed with descriptive and comparative statistics. Matched controls and normative population-based data will be used for comparison.
Ethics Patients and/or caregivers will receive written information about the study and provide written informed consent. Data that are entered into the project database will be pseudonymized to protect privacy. The benefit of the study are considered to exceed the risks.
Significance The knowledge of long-term outcomes up to adulthood in patients with anorectal malformations is limited. Particularly controlled data are scanty. This study may contribute important additional understanding and contribute to improved care of individuals with anorectal malformations.
Project timeline Autumn 2020: Ethical approval application. Identification of eligible patients. Spring 2021: All patients will be invited to participate and questionnaires sent out. Data collection.
Autumn 2021- 31 December 2026: Data collection. Collected data will be analysed and summarized in publications.
- Conditions
- Anorectal Malformations
- Medical subject headings
- Anorectal Malformations
What is being measured
The primary outcome is the main question the study is designed to answer.
Bowel function score
Bowel function score, BFS, >4 years of age (Rintala et al. J Pediatr Surg 1995;30:491-4)
Measured: 3 years
Urinary tract function
Urinary tract function evaluated with a modification of Danish Prostatic Symptom Score, >4 years of age (Kyrklund et al Dis Colon Rectum 2012;55:671-6)
Measured: 3 years
Sexual function
Sexual function evaluated with Profile of Female Sexual Function in females >18 years of age and with IIEF in males >18 years of age
Measured: 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 May 2021
- Study start1 Jan 2022
- Primary completion31 Jul 2023
- Study completion31 Jul 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Anorectal MalformationsStudies of the same condition, open and under way.
- More trials run by Karolinska InstitutetThe 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
- Cross-sectional
- Enrolment
- 300 participants (actual)
Sponsor and investigators
- Lead sponsor
- Karolinska Institutet
- Sponsor type
- University, hospital or other
- Collaborators
- Karolinska University Hospital
- Responsible party
- Principal investigator, Tomas Wester, Karolinska Institutet
- Investigators
- Tomas Wester, MD, PhD, Principal investigator, Karolinska Institutet
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04901819
- Sponsor's protocol ID
- FOR 4-1500/2021
- Other IDs
- K 2021-4578
- Status last verified
- Jan 2024
- First submitted
- 19 May 2021
- Last updated
- 23 Jan 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Svenningsson A, Gunnarsdottir A, Wester T. Maternal risk factors and perinatal characteristics of anorectal malformations. J Pediatr Surg. 2018 Nov;53(11):2183-2188. doi: 10.1016/j.jpedsurg.2018.04.021. Epub 2018 Apr 17.
PubMed 29907315von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP; STROBE Initiative. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet. 2007 Oct 20;370(9596):1453-7. doi: 10.1016/S0140-6736(07)61602-X.
PubMed 18064739Rintala RJ, Lindahl H. Is normal bowel function possible after repair of intermediate and high anorectal malformations? J Pediatr Surg. 1995 Mar;30(3):491-4. doi: 10.1016/0022-3468(95)90064-0.
PubMed 7760250Kyrklund K, Koivusalo A, Rintala RJ, Pakarinen MP. Evaluation of bowel function and fecal continence in 594 Finnish individuals aged 4 to 26 years. Dis Colon Rectum. 2012 Jun;55(6):671-6. doi: 10.1097/DCR.0b013e31824c77e4.
PubMed 22595847
Study at a glance
From the registry record, last updated by the sponsor on 23 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Longterm Outcomes of Individuals With Anorectal Malformations
- ClinicalTrials.gov ID
- NCT04901819
- Acronym / sponsor ID
- FOR 4-1500/2021
- Conditions
- Anorectal Malformations
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 300 participants (actual)
- Lead sponsor
- Karolinska InstitutetUniversity, hospital or other
- Collaborators
- Karolinska University Hospital
- Study start
- 1 Jan 2022 (actual)
- Primary completion
- 31 Jul 2023 (actual)
- Study completion
- 31 Jul 2023 (actual)
- First posted
- 26 May 2021 (actual)
- 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.
This is a cross-sectional observational study with the aim to assess longterm outcomes in a large cohort of individuals with anorectal malformations. Patients managed for anorectal malformations at Karolinska University Hospital, Stockholm, Sweden, Stockholm 1994-2017 will be reviewed and they will be invited to respond to validated questionnaires evaluating bowel function (>4 years of age), urinary tract function (>4 years of age), sexual function (>18 years of age) and quality of life (>8 years of age). Data will be analyzed with descriptive and comparative statistics.
Detailed description
Background Anorectal malformations comprise a spectrum of congenital anomalies, that range from mild anterior displacement of the anus to very complex anomalies, involving both the hindgut and the urogenital tract. The birth prevalence in Sweden is approximately 1:3000 (1). Associated anomalies are encountered in 50-60 % of individuals with anorectal malformation. Anorectal malformations are associated with tethered cord in 20-30% of patients, which may impair bowel and urinary tract function. Development of surgical techniques and neonatal care have improved survival of children with anorectal malformations over the last decades. The focus of care has shifted from survival to optimizing bowel and urinary tract function as well as reducing the negative impact on quality of life. Current surgical techniques were introduced during the early 1980's. The outcomes compare favorably with older techniques, although there is still limited information on the outcomes up to adult age. Particularly, there are limited data of composite outcomes of bowel function, urinary tract function, sexual function and quality of life in comparison to age- and gender-matched controls from the normal population. Newborn infants are often screened for tethered cord with ultrasound. It is unclear if infants with normal ultrasound also need an MRI at a later stage to exclude spinal cord anomalies. Tethered cord is frequently asymptomatic. There are conflicting data with respect to prophylactic de-tethering.
Aims The overall aim of this project was to assess composite outcomes, bowel function, urinary tract function, sexual function, and quality of life in a cross-sectional study of children with ARM managed at Karolinska University Hospital.
Specific aims
- To assess if bowel function, urinary tract function, sexual function, and quality of life is impaired in children with ARM compared with normative data.
- To assess if bowel function, urinary tract function, sexual function and quality of life correlate
- To assess if individuals with ARM and tethered cord benefit from detethering.
- To assess if ultrasound of the spinal cord and MRI are equal imaging modalities to diagnose tethered cord.
Methods Study design Cross-sectional observational study. The STROBE Statement for reporting of observational studies will be used (2).
Settings and participants All individuals managed for an anorectal malformation at Karolinska University Hospital from 1994 to 2017 will be eligible for the study. Patients and/or parents who provide informed consent and fill in the questionnaires will be included in the study. There will be 300-400 eligible patients.
Data sources and variables Demographic and clinical details will be recorded retrospectively from the medical records, including gender, birth weight, gestational age, associated syndromes and anomalies, family history, presenting symptoms, type of ARM, surgical details including postoperative complications and re-operations. Questionnaires will be sent according to age to the participants to assess bowel function, urinary tract function, sexual function, and quality of life. Questionnaires on sexual function and quality of life will not be sent to individuals with intellectual impairment, eg. Down syndrome. It will be possible to respond to the questionnaires using a digital platform. Bowel function will be assessed in individuals more than 4 years of age using a bowel function score (BFS) questionnaire (3) developed for assessment of bowel function in pediatric anorectal disorders and validated in patients and in the general Finnish population (4). Urinary tract function will be assessed in individuals more than 4 years of age with a questionnaire on lower urinary tract symptoms, with questions addressing history of urinary tract infection, urgency, urge incontinence, stress incontinence, straining to begin urination, and leakage of urine without physical activity or apparent need to urinate, based on items adapted from the previously validated Danish Prostatic Symptom Score. Profile of Sexual Female function will be used to assess sexual function in the female patients more than 18 years of age. IIEF will be used to assess sexual function in males more than 18 years of age. KIDSCREEN, a validated instrument assessing children's and adolescents subjective health and well-being, will be used to assess the quality of life in children and adolescents 8 to 18 years of age. In patients more than 18 years old, Psychological general well-being index (PGWB) will be used to assess quality of life. In a sub-study, individuals with tethered cord will be identified. The outcomes among patients with tethered cord who have undergone de-tethering will be compared with those who have not undergone an operation. In a second sub-study, spinal cord ultrasound and MRI images will be reviewed by two experienced pediatric radiologists in a blinded fashion. Correlation between the two imaging modalities will be analyzed.
Data analysis Pseudonymized data will be recorded in Excel spread sheets. Data will be analyzed with descriptive and comparative statistics. Matched controls and normative population-based data will be used for comparison.
Ethics Patients and/or caregivers will receive written information about the study and provide written informed consent. Data that are entered into the project database will be pseudonymized to protect privacy. The benefit of the study are considered to exceed the risks.
Significance The knowledge of long-term outcomes up to adulthood in patients with anorectal malformations is limited. Particularly controlled data are scanty. This study may contribute important additional understanding and contribute to improved care of individuals with anorectal malformations.
Project timeline Autumn 2020: Ethical approval application. Identification of eligible patients. Spring 2021: All patients will be invited to participate and questionnaires sent out. Data collection.
Autumn 2021- 31 December 2026: Data collection. Collected data will be analysed and summarized in publications.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 4 to 28 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
- Study population
- Individual who have undergone surgical management for anorectal malformations at Karolinska University Hospital, Stockholm, Sweden from 1994 to 2017.
Key inclusion criteria (1 listed)
- Individual who has undergone surgical management for anorectal malformation at Karolinska University Hospital 1994 to 2017.
Key exclusion criteria (1 listed)
- Individual not providing informed consent.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Bowel function score
Time frame: 3 years
Bowel function score, BFS, >4 years of age (Rintala et al. J Pediatr Surg 1995;30:491-4)
Urinary tract function
Time frame: 3 years
Urinary tract function evaluated with a modification of Danish Prostatic Symptom Score, >4 years of age (Kyrklund et al Dis Colon Rectum 2012;55:671-6)
Sexual function
Time frame: 3 years
Sexual function evaluated with Profile of Female Sexual Function in females >18 years of age and with IIEF in males >18 years of age
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Jan 2024.
- Background: PubMed 29907315Svenningsson A, Gunnarsdottir A, Wester T. Maternal risk factors and perinatal characteristics of anorectal malformations. J Pediatr Surg. 2018 Nov;53(11):2183-2188. doi: 10.1016/j.jpedsurg.2018.04.021. Epub 2018 Apr 17.
- Background: PubMed 18064739von Elm E, Altman DG, Egger M, Pocock SJ, Gotzsche PC, Vandenbroucke JP; STROBE Initiative. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet. 2007 Oct 20;370(9596):1453-7. doi: 10.1016/S0140-6736(07)61602-X.
- Background: PubMed 7760250Rintala RJ, Lindahl H. Is normal bowel function possible after repair of intermediate and high anorectal malformations? J Pediatr Surg. 1995 Mar;30(3):491-4. doi: 10.1016/0022-3468(95)90064-0.
- Background: PubMed 22595847Kyrklund K, Koivusalo A, Rintala RJ, Pakarinen MP. Evaluation of bowel function and fecal continence in 594 Finnish individuals aged 4 to 26 years. Dis Colon Rectum. 2012 Jun;55(6):671-6. doi: 10.1097/DCR.0b013e31824c77e4.
- 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.
Tomas Wester, MD, PhD principal investigator
Karolinska Institutet
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 Anorectal Malformations, run by Karolinska Institutet at 1 site in Sweden.
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 1 inclusion and 1 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: finished, as of the sponsor's last update on 23 Jan 2024. 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 Sweden. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Bowel function score (time frame: 3 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04901819, which also lists 4 linked publications.
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 23 Jan 2024.