NCT07300865 Does the Thickness of the Gastrostomy Affect the Incidence of Complications? A Prospective Randomized Single-Center Study in Children
| NCT ID | NCT07300865 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Therese Hössjer |
| Condition | Gastrostomy Complications |
| Study Type | INTERVENTIONAL |
| Enrollment | 200 participants |
| Start Date | 2025-11-20 |
| Primary Completion | 2030-01-01 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 200 participants in total. It began in 2025-11-20 with a primary completion date of 2030-01-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this interventional study is to compare two different sizes of a gastrostomy tube in children and the incidence of complications three months postoperatively. The study is questionnare-based and both the family and health care personel will fill in the formula about complications at the re-visit when the tube is changed the first time at three months postoperatively. Complications requested are: granuloma, infection, pain, dislocation and leakage.
Eligibility Criteria
Inclusion Criteria: * Scheduled for laparoscopic gastrostomy at Dep Pediatric Surgery Uppsala Akademiska University Hospital Exclusion Criteria: * Any specific reasons to avoid one size or the other (children who are supposed to get mixed food or a special medication that can obstruate the tube will recieve a thicker tube)
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07300865 clinical trial?
This trial is open to participants of all sexes, up to 15 Years, studying Gastrostomy Complications. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07300865 currently recruiting?
Yes, NCT07300865 is actively recruiting participants. Contact the research team at therese.hossjer@uu.se for enrollment information.
Where is the NCT07300865 trial being conducted?
This trial is being conducted at Uppsala, Sweden.
Who is sponsoring the NCT07300865 clinical trial?
NCT07300865 is sponsored by Therese Hössjer. The trial plans to enroll 200 participants.