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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04325984
Other study ID # 173_2018_DexaPOP
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 29, 2017
Est. completion date March 6, 2019

Study information

Verified date March 2020
Source University of Trieste
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to evaluate the analgesic properties of dexamethasone and to quantify the possible associated postoperative complications, such as wound infections and hyperglycaemia, in patients who underwent lobectomy, segmentectomy or atypical resection surgery with a mini-thoracotomy approach or video-assisted thoracoscopic surgery (VATS).


Description:

We designed an observational study, aimed to evaluate the possible reduction in morphine consumption in thoracic patients, who were administered dexamethasone compared to who didn't received the drug.

The research wants to assess the presence of additional analgesic properties, besides the well known antiemetic effect, in the intraoperative administration of dexamethasone, and the possible postoperative complications, such as wound infections and hyperglycaemia.

The rational is to ameliorate the anaesthesiological management, in particular with a view to a opioid-sparing analgesia in thoracic patients.

To do so, we enrolled thoracic patients, who underwent elective lobectomy, segmentectomy or atypical resection surgery with a mini-thoracotomy approach or video-assisted thoracoscopic surgery (VATS).

We selected two groups: one in which patients were administered dexamethasone 8 mg at the moment of induction, and the other one in which patients didn't received dexamethasone, but ondansetron 4 mg at the end of surgery. Both groups received other antiemetic drugs based on Apfel score and multimodal analgesia, comprising loco-regional analgesia, opioids and other analgesic drugs administration.

The we checked morphine consumption and Numerical Rating Scale (NRS) values for pain in the first 24 hours after surgery.

Moreover we evaluate Post-Operative Nausea and Vomiting (PONV), intra- and post-operative blood glucose levels and wound infection.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date March 6, 2019
Est. primary completion date March 6, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- BMI < 30 kg/m2

- ASA I-III

- Lobectomy, segmentectomy or atypical resection surgery with a mini-thoracotomy approach or VATS

Exclusion Criteria:

- Refusal by the patient to participate or patient unable to express his own consent

- Chronic therapy with medium-high doses of corticosteroids

- Chronic therapy with opioids

- METS = 4, defining an overall decreased cardiovascular fitness

- Urgent or emergency surgery

- Allergy to the active ingredient of the drug used

- Kidney failure at stage III or more

- Liver failure

- Pregnancy

- Drug addiction, patients with a history of drug abuse

- Corrected Qt interval (QTc) > 0,45 for males and 0,47 for women

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dexamethasone
To the Dexamethasone group, at the moment of the induction of anaesthesia, dexamethasone 8 mg is administered.

Locations

Country Name City State
Italy Cattinara Hospital Trieste

Sponsors (1)

Lead Sponsor Collaborator
University of Trieste

Country where clinical trial is conducted

Italy, 

References & Publications (6)

Doan LV, Augustus J, Androphy R, Schechter D, Gharibo C. Mitigating the impact of acute and chronic post-thoracotomy pain. J Cardiothorac Vasc Anesth. 2014 Aug;28(4):1048-56. doi: 10.1053/j.jvca.2014.02.021. Review. — View Citation

Henzi I, Walder B, Tramèr MR. Dexamethasone for the prevention of postoperative nausea and vomiting: a quantitative systematic review. Anesth Analg. 2000 Jan;90(1):186-94. — View Citation

Kakodkar PS. Routine use of dexamethasone for postoperative nausea and vomiting: the case for. Anaesthesia. 2013 Sep;68(9):889-91. doi: 10.1111/anae.12308. Epub 2013 Jul 15. — View Citation

Standards of Medical Care in Diabetes-2016: Summary of Revisions. Diabetes Care. 2016 Jan;39 Suppl 1:S4-5. doi: 10.2337/dc16-S003. Review. — View Citation

Waldron NH, Jones CA, Gan TJ, Allen TK, Habib AS. Impact of perioperative dexamethasone on postoperative analgesia and side-effects: systematic review and meta-analysis. Br J Anaesth. 2013 Feb;110(2):191-200. doi: 10.1093/bja/aes431. Epub 2012 Dec 5. Review. — View Citation

Wenk M, Schug SA. Perioperative pain management after thoracotomy. Curr Opin Anaesthesiol. 2011 Feb;24(1):8-12. doi: 10.1097/ACO.0b013e3283414175. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Glycemic changes Evaluation of intraoperative and postoperative blood glucose levels 24 hours after surgery
Other Surgical wound infection Evaluation of infectious complication after surgery: assessment of the presence of signs and symptoms of infection of the surgical wound At hospital discharge/ at first medical check if discharge was earlier than 7 days
Other Postoperative Nausea and Vomiting (PONV) Evaluation of development of postoperative nausea or vomiting, reporting the presence of episodes of nausea or vomiting in the 24 hours after the surgery 24 hours after surgery
Primary Morphine consumption Morphine dose, in milligrams, administered in the 24 hours after the surgery 24 hours after surgery
Secondary Static and dynamic Numeric Rating Scale (NRS) Evaluation of Numeric Rating Scale (NRS) for static and dynamic pain; the NRS uses scores from 0 (no pain) to 10 (worst possible pain) 24 hours after surgery
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