TY - JOUR
T1 - WONDER-01
T2 - immediate necrosectomy vs. drainage-oriented step-up approach after endoscopic ultrasound-guided drainage of walled-off necrosis—study protocol for a multicentre randomised controlled trial
AU - for the WONDERFUL study group in Japan, collaborators
AU - Sato, Tatsuya
AU - Saito, Tomotaka
AU - Takenaka, Mamoru
AU - Iwashita, Takuji
AU - Shiomi, Hideyuki
AU - Fujisawa, Toshio
AU - Hayashi, Nobuhiko
AU - Iwata, Keisuke
AU - Maruta, Akinori
AU - Mukai, Tsuyoshi
AU - Masuda, Atsuhiro
AU - Matsubara, Saburo
AU - Hamada, Tsuyoshi
AU - Inoue, Tadahisa
AU - Ohyama, Hiroshi
AU - Kuwatani, Masaki
AU - Kamada, Hideki
AU - Hashimoto, Shinichi
AU - Shiratori, Toshiyasu
AU - Yamada, Reiko
AU - Kogure, Hirofumi
AU - Ogura, Takeshi
AU - Nakahara, Kazunari
AU - Doi, Shinpei
AU - Chinen, Kenji
AU - Isayama, Hiroyuki
AU - Yasuda, Ichiro
AU - Nakai, Yousuke
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Background: With the increasing popularity of endoscopic ultrasound (EUS)-guided transmural interventions, walled-off necrosis (WON) of the pancreas is increasingly managed via non-surgical endoscopic interventions. However, there has been an ongoing debate over the appropriate treatment strategy following the initial EUS-guided drainage. Direct endoscopic necrosectomy (DEN) removes intracavity necrotic tissue, potentially facilitating early resolution of the WON, but may associate with a high rate of adverse events. Given the increasing safety of DEN, we hypothesised that immediate DEN following EUS-guided drainage of WON might shorten the time to WON resolution compared to the drainage-oriented step-up approach. Methods: The WONDER-01 trial is a multicentre, open-label, superiority, randomised controlled trial, which will enrol WON patients aged ≥ 18 years requiring EUS-guided treatment in 23 centres in Japan. This trial plans to enrol 70 patients who will be randomised at a 1:1 ratio to receive either the immediate DEN or drainage-oriented step-up approach (35 patients per arm). In the immediate DEN group, DEN will be initiated during (or within 72 h of) the EUS-guided drainage session. In the step-up approach group, drainage-based step-up treatment with on-demand DEN will be considered after 72–96 h observation. The primary endpoint is time to clinical success, which is defined as a decrease in a WON size to ≤ 3 cm and an improvement of inflammatory markers (i.e. body temperature, white blood cell count, and C-reactive protein). Secondary endpoints include technical success, adverse events including mortality, and recurrence of the WON. Discussion: The WONDER-01 trial will investigate the efficacy and safety of immediate DEN compared to the step-up approach for WON patients receiving EUS-guided treatment. The findings will help us to establish new treatment standards for patients with symptomatic WON. Trial registration: ClinicalTrials.gov NCT05451901, registered on 11 July 2022. UMIN000048310, registered on 7 July 2022. jRCT1032220055, registered on 1 May 2022.
AB - Background: With the increasing popularity of endoscopic ultrasound (EUS)-guided transmural interventions, walled-off necrosis (WON) of the pancreas is increasingly managed via non-surgical endoscopic interventions. However, there has been an ongoing debate over the appropriate treatment strategy following the initial EUS-guided drainage. Direct endoscopic necrosectomy (DEN) removes intracavity necrotic tissue, potentially facilitating early resolution of the WON, but may associate with a high rate of adverse events. Given the increasing safety of DEN, we hypothesised that immediate DEN following EUS-guided drainage of WON might shorten the time to WON resolution compared to the drainage-oriented step-up approach. Methods: The WONDER-01 trial is a multicentre, open-label, superiority, randomised controlled trial, which will enrol WON patients aged ≥ 18 years requiring EUS-guided treatment in 23 centres in Japan. This trial plans to enrol 70 patients who will be randomised at a 1:1 ratio to receive either the immediate DEN or drainage-oriented step-up approach (35 patients per arm). In the immediate DEN group, DEN will be initiated during (or within 72 h of) the EUS-guided drainage session. In the step-up approach group, drainage-based step-up treatment with on-demand DEN will be considered after 72–96 h observation. The primary endpoint is time to clinical success, which is defined as a decrease in a WON size to ≤ 3 cm and an improvement of inflammatory markers (i.e. body temperature, white blood cell count, and C-reactive protein). Secondary endpoints include technical success, adverse events including mortality, and recurrence of the WON. Discussion: The WONDER-01 trial will investigate the efficacy and safety of immediate DEN compared to the step-up approach for WON patients receiving EUS-guided treatment. The findings will help us to establish new treatment standards for patients with symptomatic WON. Trial registration: ClinicalTrials.gov NCT05451901, registered on 11 July 2022. UMIN000048310, registered on 7 July 2022. jRCT1032220055, registered on 1 May 2022.
KW - Acute necrotizing pancreatitis
KW - Drainage
KW - Endoscopy
KW - Endosonography
KW - Randomised clinical trial
KW - Stents
KW - Ultrasonography
KW - Walled-off necrosis
UR - http://www.scopus.com/inward/record.url?scp=85160187421&partnerID=8YFLogxK
U2 - 10.1186/s13063-023-07377-y
DO - 10.1186/s13063-023-07377-y
M3 - 学術論文
C2 - 37226252
AN - SCOPUS:85160187421
VL - 24
JO - Trials
JF - Trials
IS - 1
M1 - 352
ER -