OGDNCT02840929
Effect of Second-look Endoscopy on Peptic Ulcer Rebleeding in Patients With Early Resumption of Antiplatelet Agents
A study testing Second-look OGD and Esomeprazole in people with OGD and Gastric Ulcer Induced by Anti-platelet Agent, run by The University of Hong Kong at 2 sites in 2 countries.
Trial summary
OBJECTIVES: Up to 15% of patients with peptic ulcer bleeding will develop rebleeding, mainly in those with ulcers of higher-risk stigmata (i.e. Forrest class Ia to IIb). Randomized trials show that second-look endoscopy is effective in reducing rebleeding rate. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- OGD, Gastric Ulcer Induced by Anti-platelet Agent, Duodenal Ulcer Induced by Anti-platelet Agent
- What is being tested?
- Second-look OGD and Esomeprazole
- Type of treatment
- Pill or oral medicine, Injection or infusion, Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 2 participants
- Where
- 2 sitesin 2 countries
- Study dates
- Jul 2016to Sep 2017
- Phase
- Interventional
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Antiplatelet for both primary and secondary prophylaxis
- Peptic ulcers of Forrest class Ia (spurting of blood), Ib (oozing of blood), IIa (visible vessel) \& IIb (adherent clot)
Who cannot join
- Peptic ulcers of class IIc (pigmented ulcer base) \& III (clean ulcer base)
- Unsuccessful endoscopic hemostasis
- Ulcer perforation
- Gastric outlet obstruction precluding passage of scope to D2
- Malignant ulcers
- Proton pump inhibitor (PPI) allergy
- Concomitant anticoagulants
- Pregnancy
Trial locations and contacts
2 sites in 2 countries.
2 sites in 2 countries
About this study
OBJECTIVES: Up to 15% of patients with peptic ulcer bleeding will develop rebleeding, mainly in those with ulcers of higher-risk stigmata (i.e. Forrest class Ia to IIb). Randomized trials show that second-look endoscopy is effective in reducing rebleeding rate. However, whether to withhold aspirin or other anti-platelet agents (for the treatment of established cardiovascular or cerebrovascular diseases) remains controversial. Studies have shown that although continuation of anti-platelet agents reduces mortality rate due to reduced cardiovascular and cerebrovascular events, there is a marginal increase in rebleeding risk.
HYPOTHESIS: We hypothesize that continuation of aspirin or other anti-platelet agents coupled with second-look endoscopy could reduce the rebleeding rate without increasing the risk of thromboembolic events in high-risk patients.
Read the detailed description
For patients who are found to have high-risk peptic ulcers on endoscopy, they will be treated by endoscopic combination therapy including adrenaline injection and followed by either thermal coagulation or haemoclips to achieve haemostasis. Peptic ulcers of high-risk stigmata are ulcers with active bleeding, non-bleeding visible blood vessels, or adherent blood clots according to Forrest classification (Ia to IIb).
After initial haemostasis for high-risk ulcers, patients who continue to require anti-platelet agents (namely, aspirin, clopidogrel, prasugrel, or ticagrelor) for treatment or prophylaxis of cardiovascular or cerebrovascular diseases will be eligible for inclusion into study.
Eligible patients will be randomly allocated to have a scheduled second-look endoscopy 16-24 hours after initial endoscopy (i.e. the intervention group), or to receive conventional standard care (i.e. the control group). Randomization will be performed in a 1:1 ratio by computer generated random sequences.
For patients who are allocated to second-look endoscopy group, endoscopic retreatment will be performed if the ulcer shows persistence of high-risk stigmata. Retreatment again will be performed by combination of adrenaline injection follows by thermal coagulation or haemoclips. Standard conventional care will be offered to the other group of patients, in which endoscopy is indicated only in case of suspected clinical bleeding as defined in the subsequent section.
Both the intervention and control groups will receive bolus injection of proton-pump inhibitor (esomeprazole 80mg), follow by high dose infusion of 8mg/h continuously for 72 hours after initial endoscopy. Thereafter, both groups will receive oral form of proton-pump inhibitor (esomeprazole 40mg/d)
Rebleeding is suspected clinically by the presence of fresh haematemesis, or haematochezia/melaena after a normal stool, or unstable haemodynamics with systolic blood pressure ≤ 90 mmHg or pulse ≥ 100 beats/min (after ruling out other causes of shock, e.g. cardiogenic or septic shock), or a drop in haemoglobin level by 2 g/dL or more within 24 hours despite transfusion of 2 or more units of blood during the same period. If any one of the features is present, we will perform emergency endoscopy to confirm the diagnosis of recurrent peptic ulcer bleeding by either the persistence of ulcers of high-risk stigma (Forrest I to IIb) or fresh blood in the stomach). Rebleeding is only defined if it is confirmed by the presence of both clinical and endoscopic features. The findings of endoscopic high-risk stigmata on second-look endoscopy alone without the above clinical features would not be labelled as rebleeding.
During hospitalization, all patients will have close monitoring of vital signs including blood pressure, pulse and oxygen saturation. Blood tests will be taken daily for haemoglobin and renal function including urea and creatinine for the first 3 days. A designated team of gastroenterologists will assess the patients twice daily for clinical features of rebleeding, abdominal complications or development of thromboembolic complications. Cardiac enzymes (creatine kinase and troponin T), electrocardiogram and computed tomography scan of the brain will be ordered if there is any clinical suspicion of cardiovascular or cerebrovascular complications.
After observation for more than 72 hours in our medical unit, patients who have successful endoscopic haemostasis without clinical evidence of rebleeding will be either discharged or transferred to convalescent hospitals for further rehabilitation. All patients will be given esomeprazole 40mg/d on discharge and their prior anti-platelet therapies will be resumed. Patient will be contacted by our research staff at day 7 by telephone for any symptoms or discomfort. Patients can also contact us via telephone hotlines for suspected rebleeding or other urgent inquires. They will have follow-up at our specialized outpatient clinic 30 days after the primary endoscopy. Blood tests will be repeated at day 30 and drug compliance of anti-platelet therapies and esomeprazole will be checked by pill counts. If patients default their follow-up, we will contact them via phone call. In addition, we will identify any post-discharge hospitalization within the first 30 days via electronic medical records of the Hospital Authority.
- Conditions
- OGD, Gastric Ulcer Induced by Anti-platelet Agent, Duodenal Ulcer Induced by Anti-platelet Agent
- Being tested
- Second-look OGD, Esomeprazole
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Second-look OGDProcedure or surgery
Second-look OGD within 16 to 24 hours after primary OGD
EsomeprazoleDrug
| Study group | Role | What they receive |
|---|---|---|
| Second-look OGD group | Experimental | Second-look OGD within 16 to 24 hours after primary OGD, in addition to standard care (esomeprazole infusion for three days, followed by oral esomeprazole.
OGD will be offered if signs of rebleeding present) Receives: Procedure: Second-look OGD; Drug: Esomeprazole |
| Standard care group | Active comparator | Esomeprazole infusion for three days, followed by oral esomeprazole. OGD will be offered if signs of rebleeding present Receives: Drug: Esomeprazole |
What is being measured
The primary outcome is the main question the study is designed to answer.
Rebleeding
Detect difference in the rate of rebleeding within 30 days of primary esophagogastroduodenoscopy (OGD)
Rebleeding is suspected clinically by the presence of fresh haematemesis, or haematochezia/melaena after a normal stool, or unstable haemodynamics with systolic blood pressure ≤ 90 mmHg or pulse ≥ 100 beats/min (after ruling out other causes of shock, e.g. cardiogenic or septic shock), or a drop in haemoglobin level by 2 g/dL or more within 24 hours despite transfusion of 2 or more units of blood during the same period. If any one of the features is present, we will perform emergency endoscopy to confirm the diagnosis of recurrent peptic ulcer bleeding by either the persistence of ulcers of high-risk stigma or fresh blood in the stomach). Rebleeding is only defined if it is confirmed by the presence of both clinical and endoscopic features.
Measured: 30 days
Secondary outcomes (6)
cardiovascular/cerebrovascular events
Detect difference in the rate of cardiovascular/cerebrovascular events within 30 days of primary OGD
Measured: 30 days
all-cause mortality
Detect difference in the rate of all-cause mortality within 30 days of primary OGD
Measured: 30 days
days of hospital stay
Detect difference in the days of hospital stay within 30 days of primary OGD
Measured: 30 days
units of packed cell transfused
Detect difference in the units of packed cell transfused
Measured: 30 days
radiological and/or surgical interventions (as documented in Clinical Management System and medical records)
Detect difference in the need of radiological and/or surgical interventions
Measured: 30 days
gastrointestinal mortality, vascular mortality, combined gastrointestinal and vascular mortality
Detect difference in the days of gastrointestinal mortality, vascular mortality, combined gastrointestinal and vascular mortality within 30 days of primary OGD
Measured: 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jul 2016 (estimated)
- Study startJul 2016
- Primary completionSep 2017
- Study completionSep 2017
Why it stopped: Slow recruitment
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for OGDStudies of the same condition, open and under way.
- More trials run by The University of Hong KongThe 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 2 participants (actual)
Sponsor and investigators
- Lead sponsor
- The University of Hong Kong
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, LEUNG Wai Keung, The University of Hong Kong
- Investigators
- Ka Shing Cheung, MBBS, Principal investigator, Queen Mary Hospital, Hong Kong
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02840929
- Sponsor's protocol ID
- GIB1200
- Status last verified
- Nov 2017
- First submitted
- 19 Jul 2016
- Last updated
- 29 Nov 2017
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Nov 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Second-look Endoscopy on Peptic Ulcer Rebleeding in Patients With Early Resumption of Antiplatelet Agents
- ClinicalTrials.gov ID
- NCT02840929
- Acronym / sponsor ID
- GIB1200
- Conditions
- OGD, Gastric Ulcer Induced by Anti-platelet Agent, Duodenal Ulcer Induced by Anti-platelet Agent
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Slow recruitment
- Enrolment
- 2 participants (actual)
- Lead sponsor
- The University of Hong KongUniversity, hospital or other
- Study start
- Jul 2016 (actual)
- Primary completion
- Sep 2017 (actual)
- Study completion
- Sep 2017 (actual)
- First posted
- 21 Jul 2016 (estimated)
- 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.
OBJECTIVES: Up to 15% of patients with peptic ulcer bleeding will develop rebleeding, mainly in those with ulcers of higher-risk stigmata (i.e. Forrest class Ia to IIb). Randomized trials show that second-look endoscopy is effective in reducing rebleeding rate. However, whether to withhold aspirin or other anti-platelet agents (for the treatment of established cardiovascular or cerebrovascular diseases) remains controversial. Studies have shown that although continuation of anti-platelet agents reduces mortality rate due to reduced cardiovascular and cerebrovascular events, there is a marginal increase in rebleeding risk.
HYPOTHESIS: We hypothesize that continuation of aspirin or other anti-platelet agents coupled with second-look endoscopy could reduce the rebleeding rate without increasing the risk of thromboembolic events in high-risk patients.
Detailed description
For patients who are found to have high-risk peptic ulcers on endoscopy, they will be treated by endoscopic combination therapy including adrenaline injection and followed by either thermal coagulation or haemoclips to achieve haemostasis. Peptic ulcers of high-risk stigmata are ulcers with active bleeding, non-bleeding visible blood vessels, or adherent blood clots according to Forrest classification (Ia to IIb).
After initial haemostasis for high-risk ulcers, patients who continue to require anti-platelet agents (namely, aspirin, clopidogrel, prasugrel, or ticagrelor) for treatment or prophylaxis of cardiovascular or cerebrovascular diseases will be eligible for inclusion into study.
Eligible patients will be randomly allocated to have a scheduled second-look endoscopy 16-24 hours after initial endoscopy (i.e. the intervention group), or to receive conventional standard care (i.e. the control group). Randomization will be performed in a 1:1 ratio by computer generated random sequences.
For patients who are allocated to second-look endoscopy group, endoscopic retreatment will be performed if the ulcer shows persistence of high-risk stigmata. Retreatment again will be performed by combination of adrenaline injection follows by thermal coagulation or haemoclips. Standard conventional care will be offered to the other group of patients, in which endoscopy is indicated only in case of suspected clinical bleeding as defined in the subsequent section.
Both the intervention and control groups will receive bolus injection of proton-pump inhibitor (esomeprazole 80mg), follow by high dose infusion of 8mg/h continuously for 72 hours after initial endoscopy. Thereafter, both groups will receive oral form of proton-pump inhibitor (esomeprazole 40mg/d)
Rebleeding is suspected clinically by the presence of fresh haematemesis, or haematochezia/melaena after a normal stool, or unstable haemodynamics with systolic blood pressure ≤ 90 mmHg or pulse ≥ 100 beats/min (after ruling out other causes of shock, e.g. cardiogenic or septic shock), or a drop in haemoglobin level by 2 g/dL or more within 24 hours despite transfusion of 2 or more units of blood during the same period. If any one of the features is present, we will perform emergency endoscopy to confirm the diagnosis of recurrent peptic ulcer bleeding by either the persistence of ulcers of high-risk stigma (Forrest I to IIb) or fresh blood in the stomach). Rebleeding is only defined if it is confirmed by the presence of both clinical and endoscopic features. The findings of endoscopic high-risk stigmata on second-look endoscopy alone without the above clinical features would not be labelled as rebleeding.
During hospitalization, all patients will have close monitoring of vital signs including blood pressure, pulse and oxygen saturation. Blood tests will be taken daily for haemoglobin and renal function including urea and creatinine for the first 3 days. A designated team of gastroenterologists will assess the patients twice daily for clinical features of rebleeding, abdominal complications or development of thromboembolic complications. Cardiac enzymes (creatine kinase and troponin T), electrocardiogram and computed tomography scan of the brain will be ordered if there is any clinical suspicion of cardiovascular or cerebrovascular complications.
After observation for more than 72 hours in our medical unit, patients who have successful endoscopic haemostasis without clinical evidence of rebleeding will be either discharged or transferred to convalescent hospitals for further rehabilitation. All patients will be given esomeprazole 40mg/d on discharge and their prior anti-platelet therapies will be resumed. Patient will be contacted by our research staff at day 7 by telephone for any symptoms or discomfort. Patients can also contact us via telephone hotlines for suspected rebleeding or other urgent inquires. They will have follow-up at our specialized outpatient clinic 30 days after the primary endoscopy. Blood tests will be repeated at day 30 and drug compliance of anti-platelet therapies and esomeprazole will be checked by pill counts. If patients default their follow-up, we will contact them via phone call. In addition, we will identify any post-discharge hospitalization within the first 30 days via electronic medical records of the Hospital Authority.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Second-look OGD group | Experimental | Procedure: Second-look OGD, Drug: EsomeprazoleSecond-look OGD within 16 to 24 hours after primary OGD, in addition to standard care (esomeprazole infusion for three days, followed by oral esomeprazole. OGD will be offered if signs of rebleeding present) |
| Standard care group | Active comparator | Drug: EsomeprazoleEsomeprazole infusion for three days, followed by oral esomeprazole. OGD will be offered if signs of rebleeding present |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Antiplatelet for both primary and secondary prophylaxis
- Peptic ulcers of Forrest class Ia (spurting of blood), Ib (oozing of blood), IIa (visible vessel) \& IIb (adherent clot)
Key exclusion criteria (8 listed)
- Peptic ulcers of class IIc (pigmented ulcer base) \& III (clean ulcer base)
- Unsuccessful endoscopic hemostasis
- Ulcer perforation
- Gastric outlet obstruction precluding passage of scope to D2
- Malignant ulcers
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Second-look OGDSecond-look OGD within 16 to 24 hours after primary OGD | Procedure or surgery | Second-look OGD group |
| Esomeprazole | Drug | Second-look OGD group, Standard care group |
Primary outcome
Rebleeding
Time frame: 30 days
Detect difference in the rate of rebleeding within 30 days of primary esophagogastroduodenoscopy (OGD) Rebleeding is suspected clinically by the presence of fresh haematemesis, or haematochezia/melaena after a normal stool, or unstable haemodynamics with systolic blood pressure ≤ 90 mmHg or pulse ≥ 100 beats/min (after ruling out other causes of shock, e.g. cardiogenic or septic shock), or a drop in haemoglobin level by 2 g/dL or more within 24 hours despite transfusion of 2 or more units of blood during the same period. If any one of the features is present, we will perform emergency endoscopy to confirm the diagnosis of recurrent peptic ulcer bleeding by either the persistence of ulcers of high-risk stigma or fresh blood in the stomach). Rebleeding is only defined if it is confirmed by the presence of both clinical and endoscopic features.
6 secondary outcomes
cardiovascular/cerebrovascular events
Time frame: 30 days
all-cause mortality
Time frame: 30 days
days of hospital stay
Time frame: 30 days
units of packed cell transfused
Time frame: 30 days
radiological and/or surgical interventions (as documented in Clinical Management System and medical records)
Time frame: 30 days
gastrointestinal mortality, vascular mortality, combined gastrointestinal and vascular mortality
Time frame: 30 days
Results and safety
The study was stopped early (reason given: Slow recruitment). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Nov 2017.
- Individual participant dataSharing planned: No
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.
Ka Shing Cheung, MBBS principal investigator
Queen Mary Hospital, Hong Kong
2 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Second-look OGD and Esomeprazole in people with OGD and Gastric Ulcer Induced by Anti-platelet Agent, run by The University of Hong Kong at 2 sites in 2 countries.
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 2 inclusion and 8 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: stopped early, as of the sponsor's last update on 29 Nov 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in China, Hong Kong. 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 was stopped early (reason given: Slow recruitment). Results are not available in the source record.
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?
Rebleeding (time frame: 30 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 29 Nov 2017.