Evaluation of Injection Techniques in Celiac Plexus Neurolysis
Status: | Completed |
---|---|
Conditions: | Cancer, Cancer, Chronic Pain, Pancreatic Cancer |
Therapuetic Areas: | Musculoskeletal, Oncology |
Healthy: | No |
Age Range: | 19 - 89 |
Updated: | 4/21/2016 |
Start Date: | August 2013 |
End Date: | November 2014 |
Evaluation of Injection Techniques in Endoscopic Ultrasound-Guided Celiac Plexus Neurolysis (EUS-CPN)
1. To evaluate the efficacy of EUS-CPN in subjects who experience a sympathetic response
during injection when compared with subjects who do not experience sympathetic response
during injection.
EUS-CPN when performed in subjects who experience a sympathetic response during injection
will have better pain relief when compared to subjects who do not experience a sympathetic
response during injection.
during injection when compared with subjects who do not experience sympathetic response
during injection.
EUS-CPN when performed in subjects who experience a sympathetic response during injection
will have better pain relief when compared to subjects who do not experience a sympathetic
response during injection.
1. All adult patients with radiologically consistent pancreatic carcinoma referred to
Florida Hospital to undergo EUS for staging and diagnostic FNA of pancreatic mass
lesions will be eligible for study entry.
A history and physical examination will be performed to determine the character and
quality of the pain and to evaluate for any contraindication for which EUS cannot be
performed.
2. Written informed consent for study participation will be obtained at the same time as
the consent for the procedure as this study is comparing standard of care treatment
options in a regular treatment setting. Then, after giving written informed consents
and prior to the index procedure, all patients will complete the following written
assessments:
1. Standardized 11-point continuous visual analog pain scale (12)
2. Quality of life instruments: Functional Assessment of Cancer Therapy, Pancreatic
Cancer (FACT-PA) (i.e. QLQ-30 and PAN-26) (13)
3. Pain medication usage over prior 2 days (converted to equianalgesic doses of
morphine)
3. EUS will be performed in standard fashion by one of three experienced endoscopists
4. Eligible patients will be included if pancreatic carcinoma is confirmed by FNA
performed during EUS and if EUS or CT staging shows unresectability of the tumor.
Cytology evaluation of FNA is routinely provided during procedure by pathologist into
the endoscopy room at our institution.
During EUS, included patients will receive CPN in the standard fashion. Whether a
sympathetic response occurs or not during CPN, this will be documented. Sympathetic
response will be defined as change in heart rate by >10 bpm and change in BP <10mmHg.
The technique of EUS-CPN is as follows:
- Using a curvilinear array echoendosocpe, the region of the celiac plexus is
visualized from the lesser curvature of the stomach by following the aorta to the
origin of the main celiac artery. It is traced, by using counter-clockwise
rotation, to its bifurcation into splenic and hepatic arteries, with Doppler US
control if needed.
- CPN will be undertaken at the celiac space which is located between the aorta and
the celiac artery origin.
- A 20-gauge fenestrated CPN needle is used, its tip is placed slightly anterior and
cephalic to the origin of the celiac artery.
- Aspiration is first performed to ensure that vascular puncture has not occurred.
- Bupivacaine is injected first, followed by alcohol.
- Patients will be observed for 2 to 4 hours, with careful monitoring of pulse,
blood pressure and temperature.
5. Following EUS, patients will be discharged and called at home by research nurse at 24
hours for evidence of pancreatitis or other complications from the procedure, Clinical
research nurse* will also contact the patient at 1, 2, 4 weeks after EUS and then
monthly until death or 1 year. Clinical research nurse* will be blinded to the
documentation about sympathetic response. Assessment of pain scale, QOL, medication use
and side effects will be performed.
6. Following CPN, EUS operator will not be actively involved in patient care.
7. Medical decisions for each patient will be made by the patient's primary physician and
oncologist.
8. Patient can be referred for rescue CPN if the patient's primary physician and
oncologist feel that this is warranted.
Florida Hospital to undergo EUS for staging and diagnostic FNA of pancreatic mass
lesions will be eligible for study entry.
A history and physical examination will be performed to determine the character and
quality of the pain and to evaluate for any contraindication for which EUS cannot be
performed.
2. Written informed consent for study participation will be obtained at the same time as
the consent for the procedure as this study is comparing standard of care treatment
options in a regular treatment setting. Then, after giving written informed consents
and prior to the index procedure, all patients will complete the following written
assessments:
1. Standardized 11-point continuous visual analog pain scale (12)
2. Quality of life instruments: Functional Assessment of Cancer Therapy, Pancreatic
Cancer (FACT-PA) (i.e. QLQ-30 and PAN-26) (13)
3. Pain medication usage over prior 2 days (converted to equianalgesic doses of
morphine)
3. EUS will be performed in standard fashion by one of three experienced endoscopists
4. Eligible patients will be included if pancreatic carcinoma is confirmed by FNA
performed during EUS and if EUS or CT staging shows unresectability of the tumor.
Cytology evaluation of FNA is routinely provided during procedure by pathologist into
the endoscopy room at our institution.
During EUS, included patients will receive CPN in the standard fashion. Whether a
sympathetic response occurs or not during CPN, this will be documented. Sympathetic
response will be defined as change in heart rate by >10 bpm and change in BP <10mmHg.
The technique of EUS-CPN is as follows:
- Using a curvilinear array echoendosocpe, the region of the celiac plexus is
visualized from the lesser curvature of the stomach by following the aorta to the
origin of the main celiac artery. It is traced, by using counter-clockwise
rotation, to its bifurcation into splenic and hepatic arteries, with Doppler US
control if needed.
- CPN will be undertaken at the celiac space which is located between the aorta and
the celiac artery origin.
- A 20-gauge fenestrated CPN needle is used, its tip is placed slightly anterior and
cephalic to the origin of the celiac artery.
- Aspiration is first performed to ensure that vascular puncture has not occurred.
- Bupivacaine is injected first, followed by alcohol.
- Patients will be observed for 2 to 4 hours, with careful monitoring of pulse,
blood pressure and temperature.
5. Following EUS, patients will be discharged and called at home by research nurse at 24
hours for evidence of pancreatitis or other complications from the procedure, Clinical
research nurse* will also contact the patient at 1, 2, 4 weeks after EUS and then
monthly until death or 1 year. Clinical research nurse* will be blinded to the
documentation about sympathetic response. Assessment of pain scale, QOL, medication use
and side effects will be performed.
6. Following CPN, EUS operator will not be actively involved in patient care.
7. Medical decisions for each patient will be made by the patient's primary physician and
oncologist.
8. Patient can be referred for rescue CPN if the patient's primary physician and
oncologist feel that this is warranted.
Inclusion Criteria:
1. Abdominal pain typical for pancreatic cancer ( pain score ≥ 3/10)
2. Abdominal CT consistent with diagnosis of pancreatic cancer
3. Pancreatic cancer confirmed by EUS-FNA
4. Inoperable pancreatic cancer as determined during EUS or prior CT
Exclusion Criteria:
1. Age under 19 years
2. Unable to safely undergo EUS for any reason
3. Coagulopathy (Prothrombin time > 18 secs, platelet count < 80,000/ml)
4. Previous CPN or other neurolytic block that could affect pancreatic cancer-related
pain or had implanted epidural or intrathecal analgesic therapy
5. Another cause for abdominal pain such as pseudocyst, ulcer or other intrabdominal
disorder
6. Noncompliance such that the patient would not return for subsequent follow-up
7. Active alcohol or other drug use or significant psychiatric illness
8. Unable to consent
9. Non-English speaking
We found this trial at
1
site
Florida Hospital Florida Hospital is one of the country
Click here to add this to my saved trials