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Fig. 1 | Trials

Fig. 1

From: Evaluating the use of fibrin glue for sealing low-output enterocutaneous fistulas: study protocol for a randomized controlled trial

Fig. 1

Study design. Patients are randomly allocated to group A (autologous fibrin glue), group B (commercial fibrin glue) or group C (drainage cessation). After glue application or drainage cessation, fistula drainage will be evaluated for 14 days, during which a maximum of three times of glue sealing will be conducted for patients in groups A and B. Both efficacy and safety outcomes will be assessed during the whole study period.

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Trials

ISSN: 1745-6215