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Part I The establishment of doctor-nurse-patient cooperative analgesic linkage program
Part II Clinical application study of doctor-nurse-patient cooperative analgesic linkage program.
Conduct non-randomized control study in corresponding period. 80 patients from two wards which managed by the same medical and nursing team were divided into experimental and control group. Patients in the control group were received routine post-operative analgesia pump and analgesics, and functional rehabilitation, while ones in the experimental group were received doctor-nurse-patient cooperative analgesic linkage program. Evaluate the effect of pain control during rehabilitation, adverse events during rehabilitation, patients' satisfaction of pain control.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental Group | Experimental | Patients in the experimental group were received doctor-nurse-patient cooperative analgesic linkage program. |
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| control group | Active Comparator | Patients in the control group were received routine analgesic and functional rehabilitation. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Routine Dezocine injection | Drug | Dezocine 10mg were intramuscular injected at 8:00am, 4:00pm and 12:00pm. |
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| Measure | Description | Time Frame |
|---|---|---|
| movement evoked pain (Numerical rating scale) | Assess movement evoked pain during rehabilitation. Numerical rating scale is a common pain rating scale. The score ranges from 0 to 10. 0 is no pain, 10 is the most severe pain. | Each rehabilitation within 3 days after surgery |
| pain at rest (Numerical rating scale) | Assess pain at rest before rehabilitation.Numerical rating scale is a common pain rating scale. The score ranges from 0 to 10. 0 is no pain, 10 is the most severe pain. | Each rehabilitation within 3 days after surgery |
| Measure | Description | Time Frame |
|---|---|---|
| satisfaction questionare of pain control | Patients answer the questionare and rate the satisfaction of pain control. The questionnaire includes 7 items indicating different aspect of pain control. Patients rate their satisfaction using score. The score ranges from 1 to 5. 1 is extremely not satisfied, 5 is extremely satisfied. | three days after surgery |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Caijuan Xu, master | Contact | 057187783887 | xucaijuan@zju.edu.cn |
| Name | Affiliation | Role |
|---|---|---|
| Caijuan Xu, master | Second Affiliated Hospital, School of Medicine, Zhejiang University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Second Affiliated Hospital of Zhejiang University School of Medicine | Recruiting | Hangzhou | Zhejiang | 310009 | China |
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| Adjusted Dezocine injection | Drug | Dezocine 10mg were intramuscular injected at at 6:00am, 2:00pm and 10:00pm. |
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| Routine Dynastat or Flurbiprofen Axetil jinjection | Drug | Dynastat 40mg or Flurbiprofen Axetil 50mg were administrated intravenously at 9:00am, 4:00pm and 12:00pm. |
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| Adjusted Dynastat or Flurbiprofen Axetil jinjection | Drug | Dynastat 40mg or Flurbiprofen Axetil 50mg were administrated intravenously at at 6:00am, 2:00pm and 10:00pm. |
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| postoperative rehabilitation | Other | Rehabilitation was conducted at 8:00am and 2:00pm. |
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| normal analgesia pump administration | Drug | Dose of analgesia pump was added if needed. |
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| adjusted analgesia pump administration | Drug | Dose of analgesia pump was added if needed. Add one dose of analgesia pump 10 minutes before rehabilitation. |
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| the time of first bowel movement | Record the time of first bowel movement after surgery | three days after surgery |
| total dose of analgesics | record and calculate the total dose of analgesics | three days after surgery |
| pain at night (Numerical rating scale) | Asess the pain at rest during night.Numerical rating scale is a common pain rating scale. The score ranges from 0 to 10. 0 is no pain, 10 is the most severe pain. | three days after surgery |
| adverse events during rehabilitation | adverse events during rehabilitation, such as nausea, vomiting, headache, falls | three days after surgery |
| ID | Term |
|---|---|
| D010149 | Pain, Postoperative |
| D000708 | Anaplasia |
| D000377 | Agnosia |
| D010182 | Pancreatic Diseases |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D009385 | Neoplastic Processes |
| D009369 | Neoplasms |
| D010468 | Perceptual Disorders |
| D019954 | Neurobehavioral Manifestations |
| D009422 | Nervous System Diseases |
| D004066 | Digestive System Diseases |
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| ID | Term |
|---|---|
| C409945 | parecoxib |
| D012046 | Rehabilitation |
| ID | Term |
|---|---|
| D000359 | Aftercare |
| D003266 | Continuity of Patient Care |
| D005791 | Patient Care |
| D013812 | Therapeutics |
| D006296 | Health Services |
| D005159 | Health Care Facilities Workforce and Services |
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