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A randomised controlled study of patients seen in a special nurse-led clinic after gastroscopy investigation for symptoms related to indigestio

Completed
Conditions
Gastroscopy
Digestive System
gastroscopy
Registration Number
ISRCTN08109872
Lead Sponsor
Southampton University Hospitals NHS Trust (UK)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
186
Inclusion Criteria

1. Male and female patients with dyspepsia
2. Over 18 years old
3. Undergoing direct access gastroscopy

Exclusion Criteria

There are 2 stages of filtering for exclusion as follows:
1. Before gastroscopy - From referral letters/forms patients with sinister symptoms:
1.1. Anaemia
1.2. Weight loss over half a stone in three months
1.3. Haematemesis
1.4. Dysphagia
1.5. Vomiting
2. After gastroscopy:
2.1. Peptic ulcer
2.2. Tumour
2.3. Severe oesophagitis
2.4. Barrett's oesophagus
2.5. Anatomical abnormality and
2.6. Post-operative stomach

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The difference between the nurse group and GP group after intervention in: <br>1. GLADYS: 8 questions and a total low score equals to least symptoms with a minimum of 0 and maximum 20<br>2. SF-12: Six questions (3 have 2 parts and 1 has 4 parts). A total high score in this measurement denotes better health related general well being with a minimum 0 and maximum 900<br>3. UHD costs 6 months before and after gastroscopy. The UHD cost analysis is based on the price listed in the Drug Tariff (generic items) or MIMS (branded items). They are summed according to class and averaged.
Secondary Outcome Measures
NameTimeMethod
Compares before and after intervention within same group in: <br>1. GLADYS<br>2. SF-12<br>3. UHD costs
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