Who are we?


Signup for

Online registration

Log in to register
your trial

Search a trial




van CCT (UK)

van CCT (UK)

Clinical benefit and cost effectiveness of endoscopic sinus surgery (ESS) in adult patients with chronic rhinosinusitis with nasal polyps (CRSwNP)

- candidate number21047
- NTR NumberNTR4978
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR27-nov-2014
- Secondary IDsa. NL48200.018.14, b. 837002522 METC, ZonMw
- Public TitleClinical benefit and cost effectiveness of endoscopic sinus surgery (ESS) in adult patients with chronic rhinosinusitis with nasal polyps (CRSwNP)
- Scientific TitleClinical benefit and cost effectiveness of endoscopic sinus surgery (ESS) in adult patients with chronic rhinosinusitis with nasal polyps (CRSwNP)
- ACRONYMClinical Benefit of endoscopic sinus surgery in nasal polyps
- hypothesisCurrent practice variance in adult patients with chronic rhinosinusitis with nasal polyps (CRSwNP) is not efficient. Endoscopic sinus surgery (ESS) is the most common ENT operation in adults in the Netherlands. The objective of the present study is to investigate the clinical effectiveness and cost-­effectiveness of two regular used strategies (“ESS in addition to drug treatment (usual care)” versus “drug treatment alone”) in adults with CRSwNP with regard to improvement in health related quality of life (HRQoL: SNOT-­22, EQ-­5D-­5L) at 12 months follow-­up.
- Healt Condition(s) or Problem(s) studiedRhinosinusitis, Surgery, Drug, Nasal polyps
- Inclusion criteriaInformed consent
Bilateral CRSwNP (nasal polyps)
Age >17 years
Indication for endoscopic sinus surgery (primary or revision) as judged by their ENT surgeon
- Exclusion criteria1. Inability to comply with study protocol
2. Septal surgery without ESS
3. Polypectomy without ethmoidectomy
4. Turbinate surgery
5. Radical surgery
6. Denker surgery/ Draf III
7. Surgery for mucokeles
8. Systemic diseases affecting the nose
(e.g., Wegener’s, granulomatosis, sarcoid, primary ciliary dyskinesia, cystic fibrosis)
9. Antrochoanal polyps (benign polyps originating from the mucosa of the maxillary sinus).
10. Inverted papilloma and malignant polyps.
11. Acute upper or lower respiratory tract infections within 2 weeks before the inclusion visit),
12. Use of systemic corticosteroids within 4 weeks before the inclusion visit
13. Need of continuous systemic corticosteroids treatment for other disease than CRSwNP
14. Systemic diseases preventing participation in the study ( e.g. severe cardiovascular/pulmonary illness, malignancy, auto-immune disorders)
15. Pregnancy
16. Inability to be operated
17. Medication: B-blocker, systemic corticosteroid use, ACE-inhibitors
18. Aspirin intolerance
19. Alcohol/drug abuse
- mec approval receivedyes
- multicenter trialyes
- randomisedyes
- masking/blindingNone
- controlActive
- groupParallel
- Type2 or more arms, randomized
- Studytypeintervention
- planned startdate 1-jan-2015
- planned closingdate1-jan-2019
- Target number of participants238
- InterventionsEligible patients will be randomly assigned in a 1:1 ratio to one of both interventions:
1. a surgical strategy consisting of ESS in addition to drug treatment. Those assigned to the surgical strategy will be offered endoscopic sinus surgery within 6 weeks of randomization. In this study we mean by endoscopic sinus surgery the surgery as done regularly by otorhinolaryngologists in the Netherlands. We do not standardize surgery.
2. a medical strategy consisting of drug treatment alone.Those assigned to the drug treatment strategy will be seen by the otorhinolaryngologist within 6 weeks of randomization to evaluate the need for additional medical treatment. Drug treatment can be any treatment that is normally given in routine medical practice to treat CRSwNP. We do not standardize drug treatment because we want to stay closest to standard of care. The randomization will be website-­based, using block randomization and stratified by study centre.
- Primary outcomeThe primary clinical endpoint is HRQol in CRSwNP patients, measured by the SNOT-22 at 12 months follow-up. HRQol is a frequently used clinical endpoint in CRS clinical trials.
- Secondary outcomeThe effectiveness of ESS in addition to drug treatment as compared to drug treatment alone in adults with CRSwNP in the short (3-6 months) and long (12 - 24 months) term, in terms of:
• Generic HRQoL (EQ-5D-5L)
• Disease specific HRQoL and symptoms (SNOT-22)
• Endoscopic assessment of the nose
(Endoscopic assessment of the nasal cavity, graded using the Lildholt scale) Endoscopic assessment of the nose (Lund-Kennedy endoscopy scores and Modified Lund Mackay Postoperative Endoscopy Score)
• Olfactory function (Sniffin Sticks)
• Nasal obstruction (PNIF)
• Daily records cards (DRC) will be provided 2 weeks before until 2 weeks after a visit to the clinic to record daily symptoms, medication use, adverse events, healthcare resource use and related health care costs
• CRS disease control (EPOS CRS control test, NOSE test)
• Asthma control in the subgroup of patients with asthma (Asthma Control Test)
• Symptomatic exacerbations requiring further treatment including ESS identified using diaries and medical notes
• Adverse effects of drug and surgical treatment and readmissions identified using diaries and medical notes
• Healthcare resource use and related health care costs including patient time and travel costs, out-of-pocket expenditure, time off education, work and usual activities using repeated questionnaires and diaries (DRC)
- TimepointsN/A
- Trial web site
- statusplanned
- Sponsor/Initiator Academic Medical Center (AMC), Department of Ear- Nose and Throat (ENT)
- Funding
(Source(s) of Monetary or Material Support)
ZON-MW, The Netherlands Organization for Health Research and Development, Academic Medical Center (AMC), Department of Ear- Nose and Throat (ENT), European Rhinologic Society
- Publications
- Brief summaryGiven its prevalence (11% in Europe, 14,6% in the Netherlands) and the significant negative effect on quality of life, the diagnosis and treatment of chronic rhinosinusitis (CRS) is associated with a significant medical resource use and societal economic burden. CRS has been shown to have a negative impact on most aspects of Health related Quality of Life and has a greater impact on HRQoL than chronic heart failure, angina, diabetes or back pain. CRS is the most common reason for surgery (ESS) in adult patients in the otorhinolaryngological practice with around 18,000 ESS performed in The Netherlands yearly (2010 data stichting hospital data (DHD)). CRS can be divided into the more serious disease CRS with nasal polyps (CRSwNP) (prevalence 1-­4%) and CRS without nasal polyps (CRSsNP). Around 70% of the ESS is done in patients with CRSwNP. Surgery requires anaesthesia and convalescence and has a small but relevant risk of serious (intracranial) complications. At present it is unknown whether ESS added to drug treatment offers significant benefits over drug treatment alone. The objective of this open multi-centre randomized trial is to investigate whether these two regular used strategies in adults with CRSwNP differ in improvement in health related quality of life (SNOT-22, EQ-5D-5L) at 12 months follow-up (primary outcome). Furthermore both strategies will be compared with respect to cost-effectiveness. Based on the primary outcome measurement, a sample size of 238 patients will have 90% power to detect a difference in means of 8.9, standard devitation 20.0 using a 0.05 two-sided significance level. Eligible patients will be randomized to a. ESS within 6 weeks in addition to drug treatment, or b. drug treatment alone. We will need 2 months start-up, 18 months of inclusion and 24 months follow-up.
- Main changes (audit trail)
- RECORD27-nov-2014 - 13-mrt-2015

  • Indien u gegevens wilt toevoegen of veranderen, kunt u een mail sturen naar