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CompletedNCT04703257Metamizole003Updated Jan 6, 2023

Evaluation of the Added Value of Metamizole to Standard Postoperative Treatment After Ambulant Shoulder Surgery

An interventional study of Metamizole and Placebo in Postoperative Pain, Analgesia and Surgery, sponsored by Jessa Hospital. Completed at 1 site in Belgium. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2023-01-06.

Sponsored by Jessa Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
110
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study aims to investigate if the combination of metamizole and paracetamol is superior in reducing post-operative pain on day 1 after ambulatory shoulder surgery where the use of NSAIDs is prohibited compared to paracetamol treatment.

Therefore, a monocenter, prospective, double-blind, randomized controlled superiority trial will be designed to investigate the superiority of the combination of metamizole and paracetamol compared to paracetamol treatment in patients undergoing arthroscopic shoulder surgery with tendon repair.

Read the detailed description

In an ambulatory setting, good post-operative analgesia is challenging because patients have to control pain at home by themselves, in the absence of hospital staff. Moreover, there is a limit in the type of analgesia that is available (i.e. no strong opioids) as well as in the route of administration (i.e. no epidural, intravenous, subcutaneous, or intramuscular route) at home. Nowadays a multimodal approach based on a combination of paracetamol, non-steroidal anti-inflammatory drugs (NSAIDs) and, if necessary, weak opioids to control pain has been advocated in the ambulatory setting. Local and regional anesthesia also has been advocated in the ambulatory setting to relieve pain for 8 to 24 hours after surgery. Despite this multimodal pain therapy, the prevalence of outpatients suffering from moderate to severe acute postoperative pain at home remains high and varies from 9 to 40%. More specifically, some patients seem to be at high risk to develop moderate to severe pain on the fourth postoperative day, among which patients undergoing arthroscopic shoulder surgery.

Besides this high prevalence, recent findings suggest that the use of NSAIDs is detrimental to tendon healing, especially in early stages. This negative impact is due to its effect on both proliferation and migration of tendon cells, as well as the inflammation reaction involved in the healing process and the bone growth necessary for tendon-to-bone healing. Healing of injured tendon proceeds through three phases: inflammation, regeneration, and remodeling/maturation. The initial phase involves an inflammatory response, in which the pro-inflammatory cyclooxygenase-2 (COX-2)/prostaglandin E2 (PGE-2) pathway is of major importance. In the regenerative phase of a tendon injury, tendon cells migrate towards a repair site, proliferate and deposit extracellular matrix (ECM) in the tissue. The expression of paxillin, a positive regulator of cell mobility, is downregulated by ibuprofen, resulting in inhibited tendon cell migration. Moreover, treatment decreases DNA synthesis and gene expression in tendon cells, harming proliferation, and interfering with normal processes of ECM remodeling. Furthermore, the resulting p21CYP1 expression and decreased Rb protein phosphorylation are associated with inhibited proliferation. Additionally, the inhibition of COX-enzymes associated with PGE-2 inhibition may lead to impaired osteoblast differentiation, essential for tendon-to-bone healing.

On top of that, NSAIDs are not always sufficiently effective, can have numerous contraindications, and are therefore not suitable in up to 25% of all patients. These controversies implicate the need for alternative pain therapy. Metamizole (dipyrone) is a non-opioid compound with strong analgesic, antipyretic, and spasmolytic effects. The analgesic efficacy of intravenous or intramuscular metamizole for pain relief after inpatient surgery is well described. Recently, we showed in a prospective, double-blind, randomized controlled trial that the combination of paracetamol and metamizole is equally effective in the treatment of acute postoperative pain at home after ambulatory surgery compared to paracetamol and ibuprofen. Moreover, patient satisfaction was equal in both groups, as well as the reported side effects.

Multiple mechanisms are involved in the antinociceptive effects of metamizole. More particularly, the inhibition of COX-1 and -2 enzymes and the activation of the endocannabinoid and opioidergic system. This seems partly similar to the working mechanism of NSAIDs, suggesting a theoretical presumption that metamizole also harms tendon repair. However, metamizole is not classified as an NSAID and no detrimental effect of metamizole on tendon healing and no link between metamizole and the previously described mechanism has been reported in the literature. The most important advantage of metamizole compared with NSAIDs is its favorable gastro-intestinal and cardiovascular side effect profile. Therefore, replacing NSAIDs with metamizole in the standard approach in surgeries where NSAIDs are contraindicated such as shoulder arthroscopies with tendon repair may increase the overall suitability of postoperative pain therapy.

02

Conditions studied

  • Postoperative Pain
  • Analgesia
  • Surgery

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Keywords

  • ambulant shoulder surgery
  • post-operative pain
  • recovery
03

In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's enrollment of 110 is above the median of 75 across 4,344 interventional studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Jessa Hospital is the lead sponsor of 85 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients aged between 18 and 75 years
  • ASA classification 1, 2 or 3
  • Bodyweight > 50 kg
  • Undergoing ambulatory arthroscopic shoulder surgery and with a contraindication to NSAID (SAD ± ACJ excision or decompression, decompression + biceps tenodesis, SLAP repair, Bankart repair, rotator cuff repair)

Exclusion criteria

Exclusion Criteria:

  • Not meeting inclusion criteria
  • Cognitive impairment or no understanding of the Dutch language
  • Preoperative pharmacological pain treatment and/or a history of chronic pain excluding shoulder pain
  • Allergy to or contraindication for taking the study medication (e.g. paracetamol or metamizole)
  • Porphyria
  • Pregnancy or lactation
  • A history of severe renal, hepatic, pulmonary or cardiac failure
  • A history of substance abuse, or use of medication with a suppressive effect on the central nervous system
  • Hypotension
  • Hematological disease
  • Use of anti-rheumatic drugs
  • Rhinosinusitis or nasal polyposis
  • Glucose-6-phosphate dehydrogenase deficiency
  • Fever or other signs of infection
  • Refusal of an interscalene block
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
110 participants (actual)

Study arms

  • Placebo comparator
    Control group

    Patients in the control group will be instructed to take a placebo tablet three times a day for four days and patients will be instructed to take 1000 mg paracetamol orally four times a day for four days.

    Drug: Placebo

  • Active comparator
    Intervention group

    Patients in the experimental group will be instructed to take metamizole 1000 mg orally three times a day for four days patients will be instructed to take 1000 mg paracetamol orally four times a day for four days.

    Drug: Metamizole

Interventions

  • DrugMetamizole

    Patients in the experimental group will be instructed to take metamizole 1000 mg orally three times a day for four days patients will be instructed to take 1000 mg paracetamol orally four times a day for four days. .

  • DrugPlacebo

    Patients in the control group will be instructed to take a placebo tablet three times a day for four days and patients will be instructed to take 1000 mg paracetamol orally four times a day for four days.

06

What researchers measure

Primary outcomes

  1. Postoperative pain at movement

    Postoperative pain intensity at movement measured by an 11-point Numeric Rating Scale (NRS), where 0: no pain and 10: worst imaginary pain, on postoperative day 1.

    Time frame: 24 hours after the surgery

Secondary outcomes

  1. Quality of recovery

    Quality of Recovery measured by the 1-item Global Surgical Recovery (GSR) index which represents a single question about the extent to which patients consider themselves to be recovered from surgery (0-100%) at baseline and days 7, 14, 28 and 3 months postoperatively.

    Time frame: at baseline and days 7, 14, 28 and 3 months postoperatively

  2. Quality of Recovery

    Measured with the EuroQol (EQ5D) questionnaire, which is non-disease specific instrument developed for describing and valuing health-related quality of life, at baseline and days 7, 14, 28 and 3 months postoperatively

    Time frame: at baseline and days 7, 14, 28 and 3 months postoperatively

  3. Postoperative pain

    Postoperative pain intensity at rest and at movement measured by an 11-point Numeric Rating Scale (NRS) where 0: no pain and 10: worst imaginary pain) at baseline, at discharge and at day 1, 2, 3, 4, 7, 14, 28 and at 3 months.

    Time frame: at baseline, at discharge, and day 1, 2, 3, 4, 7, 14, 28, and 3 months postoperatively.

  4. Simple shoulder test

    Simple shoulder test (SST) measured at baseline and days 7, 14, 28 and 3 months postoperatively.

    Time frame: at baseline and days 7, 14, 28, and 3 months postoperatively.

  5. Adherence

    Adherence to studymedication on day 1, 2, 3 and 4 postoperatively

    Time frame: day 1, 2, 3 and 4 postoperatively

  6. Adverse effects

    Adverse effects of the studymedication

    Time frame: throughout study completion, e.g. 3 months postoperatively

  7. Piritramide

    The total amount of piritramide used in the PACU

    Time frame: after surgery until discharge of PACU (up to 3 hours after surgery)

  8. Rescue medication

    The use of rescue medication (tramadol) at home on day 1, 2 ,3 and 4 postoperatively (yes/no)

    Time frame: on day 1, 2, 3 and 4 postoperatively

  9. Satisfaction of the patient

    Satisfaction with study medication, surgery and hospital care and telephone follow-up measured at day 7 and 3 months postoperative measured by an 11-point Numeric Rating Scale (NRS) where 0: totally unsatisfied and 10: totally satisfied

    Time frame: at day 7 and 3 months postoperatively

07

Study locations

1 site
  • Anesthesiology Jessa hospital
    Hasselt, 3500, Belgium
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04703257
Lead sponsor
Jessa Hospital
Responsible party
Stessel Björn (Dr, Principal Investigator, Jessa Hospital) — Principal investigator
First posted
Jan 11, 2021
Start date
Feb 26, 2021
Primary completion
Dec 21, 2022
Completion
Dec 21, 2022
Last update
Jan 6, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

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